About dbCRID

  • dbCRID (Database of Chromosomal Rearrangements In Diseases) is the largest database of curated database of human Chromosome rearrangements and associated diseases.
  • Current release: v 0.9 (06/30/2010).
  • Please direct questions and comments to dbCRID@biolead.org.
  • Related Databases

  • AtlasGeneticsOncology, Atlas of Genetics and Cytogenetics in Oncology and Haematology
  • ChimerDB 2.0, A knowledgebase for fusion genes updated
  • CytoD 1.0, A database of cytogenetic abnormalities.
  • DACRO, A disease-Associated Chromosomal Rearrangements Online.
  • Decipher, , A Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources
  • HYBRIDdb,A database of hybrid genes in the human genome.
  • Mitelman, A database of Chromosome Aberrations and Gene Fusions in Cancer.
  • SKY/M-FISH &CGH, A public platform for investigators to share and compare their molecular cytogenetic data.
  • TICdb, A database of Translocation breakpoints In Cancer.
  • References

  • Kong F, Zhu J, Wu J, Peng J, Wang Y, Wang Q, Fu S, Yuan L and Li T: dbCRID: a database of chromosomal rearrangements in human diseases. Nucleic Acids Res. [PubMed] [Full-text]
  • Search Results
    Event ID Karyotype Precision Case ID Disease
    10044 del(x)(p21pter) C 10170 McLeod Syndrome
    10045 del(x)(p21pter) C 10171 McLeod Syndrome
    10063 del(X)(p22.12pter) C 10341
    10065 del(x)(p21.1pter) C 10345
    10066 del(x)(p21.1pter) C 10346
    10071 del(X)(p11.4p11.2) C 10362 Turner Syndrome
    10291 del(x)(q26qter) C 10433 Down Syndrome
    10344 del(X)(q28q28) A 10624 Nephrogenic Diabetes Insipidus
    11253 del(X)(q28q28) A 10626 Nephrogenic Diabetes Insipidus
    10358 del(X)(q27.3) B 10682 Fragile-X Syndrome
    10398 del(X)(p21.1p21.1) A 10862 Duchenne Muscular Dystrophy
    11246 dup(X)(q26.1q27.3) C 13322
    10400 del(X)(p21.1p21.1) A 10865 Duchenne Muscular Dystrophy
    10401 del(X)(p21.1p21.1) A 10868 Duchenne Muscular Dystrophy
    10402 del(X)(p21.1p21.1) A 10870 Duchenne Muscular Dystrophy
    10403 del(X)(p11.23p11.23) A 10871 Wiskott-Aldrich Syndrome
    10410 del(X)(qterq13.3) C 10895
    10411 del(X)(qterq21) C 10897
    10412 del(X)(qterq23) C 10899
    10413 del(X)(qterq24) C 10900
    10414 del(X)(qterq26) C 10901
    10415 del(X)(qterq27) C 10902
    10613 del(X)(p21.1p21.1) B 10915 Duchenne Muscular Dystrophy and Profound Mental Retardation
    10646 del(x)(q26.2qter) C 11056 Premature Ovarian Failure
    10647 del(x)(q23q28) C 11057 Premature Ovarian Failure
    10648 del(x)(q21.2qter) C 11058 Premature Ovarian Failure
    10652 del(X)(q12q12) A 11064 Androgen-insensitivity Syndrome
    10653 del(X)(q12q12) A 11066 Androgen-insensitivity Syndrome
    10656 del(X)(q27.1q27.1) A 11080 Mental Retardation
    10657 del(X)(p21.1p21.1) A 11098 Duchenne Muscular Dystrophy
    10675 del(X)(q21.1q21.1) A 11163 Muscular Dystrophy
    10676 del(X)(q21.1, q21.1) A 11165 Muscular Dystrophy
    10677 del(X)(q21.1q21.1) A 11166 Muscular Dystrophy
    10696 del(X)(p21.2p21.2) B 11222 Becker Muscular Dystrophies
    10716 del(X)(p22.12p22.12) A 11314
    10738 del(X)(q21q21) C 11387 Premature Ovarian Failure
    10771 del(x)(q28q28) A 11602 Rett Syndrome
    10773 del(x)(q28q28) A 11604 Rett Syndrome
    10775 del(x)(q28q28) A 11609 Rett Syndrome
    10776 del(x)(q28q28) A 11610 Rett Syndrome
    10778 del(x)(q28q28) A 11611 Rett Syndrome
    10779 del(x)(q28q28) A 11612 Rett Syndrome
    10780 del(x)(q28q28) A 11613 Rett Syndrome
    10791 del(x)(q28q28) A 11639 Rett Syndrome
    10792 del(x)(q28q28) A 11640 Rett Syndrome
    10793 del(x)(q28q28) A 11641 Rett Syndrome
    10794 del(x)(q28q28) A 11642 Rett Syndrome
    10817 del(X)(p22.31p22.33) C 11711
    10831 del(X)(p22.3p22.3) C 11761
    10856 del(X)(p22.31pter) B 11849 Malignant Lymphoma
    10863 del(X)(p21p22.3) C 11865 Juvenile Idiopathic Arthritis, Mental Retardation
    10877 del(x)(p21.2p21.2) A 11910 Duchenne Muscular Dystrophy
    10878 del(x)(p21.2p21.2) A 11911 Duchenne Muscular Dystrophy
    10887 del(X)(p21.1p21.1) A 11994 Duchenne Muscular Dystrophy
    10897 del(X)(p11.2p11.2) B 12018 Synovial Sarcoma
    10906 del(X)(p11.4p21.1) A 12042 Chronic Granulomatous Disease
    10909 del(x)(q22q22) B 12055 Alport Syndrome
    10911 del(x)(q22q22) C 12056 Alport Syndrome
    10924 del(X)(p22p22) C 12080 Microphthalmia with Linear Skin Defects Syndrome
    11005 del(x)(q22q22) A 12288 Diffuse Esophageal Leiomyomatosis
    11011 del(11)(q11.2qter) C 12346
    11012 del(x)(p11.2pter) C 12348
    11017 del(X)(p11.4p21.1) A 12379 Duchenne Muscular Dystrophy, McLeod Syndrome, Chronic Granulomatous Disease and XIRP
    11018 del(X)(q28q28) A 12393
    11035 del(x)(q28q28) A 12463 Emery-Dreifuss Muscular Dystrophy
    11036 del(x)(q28q28) A 12464 Emery-Dreifuss Muscular Dystrophy
    11056 del(X)(q22.1q22.1) A 12552 Fabry Disease
    11057 del(X)(q22.1q22.1) A 12553 Fabry Disease
    11058 del(X)(q22.1q22.1) A 12554 Fabry Disease
    11059 del(X)(q22.1q22.1) A 12555 Fabry Disease
    11064 del(X)(q28q28) A 12588 X-linked Adrenoleukodystrophy
    11065 del(X)(q28q28) A 12590 X-linked Adrenoleukodystrophy
    11067 del(X)(q28q28) A 12594 Adrenomyeloneuropathy
    11068 del(X)(q28q28) A 12595 Hydrocephalus
    11070 del(X)(q28q28) A 12597 Hydrocephalus
    11071 del(X)(p22.3pter) C 12600 Mild Mental Retardation Range
    11072 del(X)(p22.3pter) C 12601
    11083 del(X)(p22.1pter) C 12678 Non-Hodgkin Lymphoma
    11104 del(X)(p21.1p21.1) A 12748 Becker muscular dystrophy
    11114 del(X)(p22.13p22.13) A 12764 Early Onset Epileptic Encephalopathy
    11115 del(X)(p22.13p22.13) C 12765 Early Onset Epileptic Encephalopathy
    11116 del(X)(p22.13p22.13) A 12766 Early Onset Epileptic Encephalopathy
    11117 del(X)(p22.3p22.3) C 12767 Early Onset Epileptic Encephalopathy
    11120 del(X)(q26.3q26.3) A 12784 Lesch-Nyhan Syndrome
    11121 del(X)(q26.3q26.3) A 12785 Lesch-Nyhan Syndrome
    11122 del(X)(q26.3q26.3) A 12786 Lesch-Nyhan Syndrome
    11125 del(x)(q26.3q27.3) C 12806 Fragile X syndrome
    11126 del(x)(q26.3q27.3) C 12807
    11156 del(X)(q27.3q27.3) A 12923 Mental Impairment
    11157 del(X)(q27.3q27.3) B 12924 Mental Impairment
    11181 del(x)(p22.3pter) C 13019
    11185 del(x)(q21qter) C 13031
    11194 del(x)(p22.3pter) C 13080
    11196 del(x)(q21.1q21.31) C 13091 Tapetochoroidal Dystrophy
    11197 del(x)(q21.2q21.31) C 13092 Tapetochoroidal Dystrophy
    11198 del(x)(q21.2q21.31) C 13093 Tapetochoroidal Dystrophy
    11199 del(x)(q21.1q21.2) C 13094
    11200 del(x)(q21.2q21.2) C 13095 Tapetochoroidal Dystrophy
    11201 del(x)(q21.1qter) C 13096 Tapetochoroidal Dystrophy
    11202 del(x)(q21.1q21.33) C 13097 Tapetochoroidal Dystrophy
    11203 del(x)(q21.1q21.32) C 13098 Tapetochoroidal Dystrophy
    11204 del(x)(q21.1q21.31) C 13099 Tapetochoroidal Dystrophy
    11205 del(x)(q21.1q21.2) C 13100 Tapetochoroidal Dystrophy
    11208 del(x)(q23qter) C 13123 Infertile
    11213 del(x)(q24qter) C 13160
    11249 del(X)(p21.1p21.1) A 13329 Duchenne Muscular Dystrophy
    10319 dup(X)(q28) C 12233 Non-syndromic Mental Retardation
    10243 dup(X)(p22.11p22.32) C 10756
    10250 dup(X)(q27.1;q27.1q27.1) A 11081 Growth Hormone Deficiency
    10258 dup(X)(q25q28) C 11318 Acute Lymphoblastic Leukemia
    10266 dup(X)(q22.2q22.2) A 11420 Pelizaeus-Merzbacher Disease
    10267 dup(X)(q22.1q22) A 11421 Pelizaeus-Merzbacher Disease
    10268 dup(X)(q22.2q22.2) A 11422 Pelizaeus-Merzbacher Disease
    10269 dup(X)(q22.2q22.2) A 11423 Pelizaeus-Merzbacher Disease
    10270 dup(X)(q22.1q22) A 11424 Pelizaeus-Merzbacher Disease
    10271 dup(X)(q22q22.2) A 11425 Pelizaeus-Merzbacher Disease
    10272 dup(X)(q22.2q22.2) A 11426 Pelizaeus-Merzbacher Disease
    10273 dup(X)(q22.1q22.2) A 11427 Pelizaeus-Merzbacher Disease
    10274 dup(X)(q22.2q22.2) A 11428 Pelizaeus-Merzbacher Disease
    10275 dup(X)(q22.2q22.2) A 11430 Pelizaeus-Merzbacher Disease
    10276 dup(X)(q22.2q22.2) A 11432 Pelizaeus-Merzbacher Disease
    10277 dup(X)(q22.2q22.3) A 11434 Pelizaeus-Merzbacher Disease
    10278 dup(X)(q22.1q22.3) A 11437 Pelizaeus-Merzbacher Disease
    10292 dup(X)(q22.2q22.2) A 11615 Pelizaeus-Merzbacher Disease
    10295 dup(X)(q22.2q22.2) A 11623 Pelizaeus-Merzbacher Disease
    10296 dup(X)(q22.2q22.2) A 11625 Pelizaeus-Merzbacher Disease
    10298 dup(X)(q22.1q22.2) C 11630 Pelizaeus-Merzbacher Disease
    10299 dup(X)(q22.1q22.3) C 11631 Pelizaeus-Merzbacher Disease
    10303 dup(X)(p21.2p21.2) A 11741
    10309 dup(X)(p22.31;p22p22.32) B 11843 Mental Retardation Syndrome
    10312 dup(X)(q28) C 11967 Lubs X-linked Mental Retardation Syndrome
    10313 dup(X)(q28) C 11970 Lubs X-linked Mental Retardation Syndrome
    10314 dup(X)(q28) C 11973 Mental Retardation Syndrome
    10315 dup(X)(q28) C 11975 Mental Retardation Syndrome
    10316 dup(X)(q22.3;q22.3q22.3) A 12019 Mowat-Wilson Syndrome
    10335 dup(X)(q28q28) A 12317
    10336 dup(X)(q28q28) A 12320
    10337 dup(X)(q28q28) A 12323
    10338 dup(X)(q28q28) A 12327
    10342 dup(X)(q28q28) A 12331
    10343 dup(X)(q28q28) A 12332
    10344 dup(X)(q28q28) A 12333
    10345 dup(X)(q28q28) A 12334
    10346 dup(X)(q28q28) A 12335
    10347 dup(X)(q28q28) A 12336
    10348 dup(X)(q28q28) A 12337
    10349 dup(X)(q28q28) A 12356
    10350 dup(X)(q28q28) A 12364
    10351 dup(X)(q28q28) A 12369
    10352 dup(X)(q28q28) A 12373
    10353 dup(X)(q28q28) A 12375
    10354 dup(X)(q28q28) A 12378
    10355 dup(X)(q28q28) A 12382
    10356 dup(X)(q28q28) A 12383
    10357 dup(X)(q28q28) A 12385
    10358 dup(X)(q28q28) A 12386
    10359 dup(X)(q28q28) A 12387
    10360 dup(X)(q28q28) A 12388
    10361 dup(X)(q28q28) A 12389
    10362 dup(X)(q28q28) A 12390
    10363 dup(X)(q28q28) A 12391
    10364 dup(X)(q28q28) A 12392
    10365 dup(X)(q28q28) A 12394
    10366 dup(X)(q28q28) A 12395
    10367 dup(X)(p21pter) C 12440
    10373 dup(X)(q22.1q22.1) A 12551 Fabry Disease
    10379 dup(X)(q26.3;q26.3q26.3) A 12787 Lesch-Nyhan Syndrome
    10384 dup(X)(q28;q28q28) A 12974
    10385 dup(X)(q28;q28q28) A 12975
    10386 dup(X)(q28;q28q28) A 12975
    10387 dup(X)(q28;q28q28) A 12976
    10389 dup(X)(p22.2) C 13185
    10002 ins(X; 11)(q24;q23.3q21) C 10192 Acute Myelocytic Leukemia
    10010 ins(X;11)(q22;q13q25) B 10880 Acute Myelocytic Leukemia
    10036 ins(x)(q28) A 11609 Rett Syndrome
    10041 ins(X;11)(q24;q13q23) B 11908 Acute Myelocytic Leukemia
    10043 inv(X)(p22.11p22.32) C 10757
    10045 inv(X)(p21.1;q22) B 10833 Mental Retardation
    10049 inv(X)(p11.1q13.1) C 10863 Mental Retardation Syndrome
    10613 inv(X)(p21.2q22.2) A 10915 Duchenne Muscular Dystrophy and Profound Mental Retardation
    10625 inv(X)(p21.3q27.1) B 11079 Mental Retardation
    10664 inv(X)(p22.3q27) C 11794
    10698 inv(X)(q28q28) A 12327
    10699 inv(X)(p11.2q21.3) C 12349
    10700 inv(X)(p11.2q21.3) C 12350 Mental Retardation Syndrome
    10002 r(X)(p11.21q13.2) C 10439 Kabuki Syndrome
    10004 r(X)(p11.3q13) C 10527
    10012 r(X)(p22q21) C 12081 Microphthalmia with Linear Skin Defects Syndrome
    10016 r(X)(p11q11) C 12827 Ullrich-Turner Syndrome
    10045 t(X;Y)(q22;p11) C 10069
    10101 t(8;X)(p21.2;q13) C 10144 Aarskog Syndrome
    10131 t(X;13)(q21;q12) C 10177 Mental Retardation Syndrome
    10181 t(X;18)(p11.2;q11.2) C 10241 Synovial Sarcoma
    10211 t(X;11)(q24;q23) C 10293 Acute Myelocytic Leukemia-M3
    10237 t(X;3)(q25;q27.2) B 10331 Lowe Syndrome
    10273 t(X;Y)(p22.3;q11.2) C 10387
    10289 t(X;18)(p11;q11) C 10418 Synovial Sarcomas
    10300 t(X;15)(p21;p10) C 10441 Killer-cell Lymphoma/leukemia
    10302 t(X;3)(p21;p25) C 10444 Killer-cell Lymphoma/leukemia
    10343 t(X;18)(p11.2;q11.2) B 10507 Synovial Sarcoma
    10344 t(X;18)(p11.2;q11.2) B 10508 Synovial Sarcoma
    10367 t(X;12)(q24;q15) C 10537 Mental Retardation Syndrome
    10385 t(X;7)(q28;q34) A 10557 T-Cell Prolymphocytic Leukemia
    10388 t(X;5)(q13;q13) C 10560 Hepatocellular Carcinoma
    10395 t(X;11)(q10;p10) C 10573 Hepatocellular Carcinoma
    10408 t(X;21)(p11.2;q22.3) C 10588 Mental Retardation Syndrome
    10525 t(X;1)(p11;q21) C 10783 Renal Cell Carcinoma
    12111 t(X;1)(q21;q44) C 10829 Premature Ovarian Failure
    10587 (X;14)(p22.31;p11.1) C 10861 Mental Retardation Syndrome
    10591 t(X ;4(q21.2;p16.3) C 10873
    10597 t(X;3)(q22;p21) C 10880 Acute Myelocytic Leukemia
    10598 t(X;11)(q24;q23) A 10886 Acute Myelocytic Leukemia
    10604 t(X;15)(q13.3;p11) C 10896
    10605 t(X;13)(q22;q32) C 10898
    10624 t(10;X)(q24;p22) C 10930
    10625 t(X;3)(p11.2;p25) B 10935 Mental Retardation Syndrome
    10629 t(X;17)(q27;q22) C 10941
    10632 t(X;Y)(p22.3;q11.2) C 10944
    10634 t(X;Y)(q28;q11.21) C 10946
    10636 t(x, 15)(q28, q12) C 10964 Prader-Willi Syndrome
    10696 t(x, x)(q22, p21) C 11060 Premature Ovarian Failure
    10697 t(x, 9)(q22, p21) C 11060 Premature Ovarian Failure
    10713 t(X;11)(q26.3;p12) C 11087
    10714 t(X;7)(q27.3;q22.3) C 11088
    10715 t(X;6)(p11.2;p21.1) C 11089
    10716 t(X;6)(q28;p12) C 11090
    10730 t(X;18) (p11.22; q11.2) A 11114 Synovial Sarcomas
    10731 t(X;18) (p11.22; q11.2) A 11115 Synovial Sarcomas
    10744 t(X;6)(q26;q23) C 11140 Premature Ovarian Failure
    10766 t(X; 22)(q27;q11) A 11187 Neural Tube Defects
    10811 t(X;11)(q21;q23) A 11244 B-Cell Chronic Lymphoblastic Leukemia
    10857 t(X;9)(p22.2;q21.12) A 11307 Hypomagnesemia with Secondary Hypocalcemia
    10873 t(X;15)(p11.3;q26) C 11340 Multiple Malformations
    10876 t(X;22)(p22.1;p11.1) C 11346
    10877 t(X;6)(p11.2;q21) C 11347
    10879 t(X;18)(p11;q11) C 11353 Synovial Sarcoma
    10909 t(X;5)(q21;q35) C 11389 Premature Ovarian Failure
    10910 t(X;3)(q21;p21) C 11390 Premature Ovarian Failure
    10911 t(X;1)(q21;p31.1) C 11391 Premature Ovarian Failure
    10912 t(X;2)(q21;q23) C 11392 Premature Ovarian Failure
    10913 t(X;4)(q21;q31.3) C 11393 Premature Ovarian Failure
    10914 t(X;12)(q21;p13) C 11394 Premature Ovarian Failure
    10915 t(X;3)(q21.2;q12) C 11395 Premature Ovarian Failure
    10916 t(X;3)(q21.2;q12) C 11396 Premature Ovarian Failure
    10917 t(X;19)(q21.2;p13.3) C 11397 Premature Ovarian Failure
    10918 t(X;9)(q21.2;q22) C 11398 Premature Ovarian Failure
    10919 t(X;16)(q21.2;p12) C 11399 Premature Ovarian Failure
    10920 t(X;9)(q21.3;q34) C 11400 Premature Ovarian Failure
    10921 t(X;3)(q22.3;q12.3) C 11401 Premature Ovarian Failure
    10922 t(X;12)(q22;p11.2) C 11402 Premature Ovarian Failure
    10923 t(X;18)(q22.3;q23) C 11403 Premature Ovarian Failure
    10924 t(X;4)(q24;q35) C 11404 Premature Ovarian Failure
    10925 t(X;15)(q24;p13) C 11405 Premature Ovarian Failure
    10932 t(X;15)(q22.3;q11.2) C 11418
    10980 t(X;2)(q12;p23.2) A 11494 Anaplastic Large Cell Lymphoma
    11001 t(X;18)(p11;q11) B 11528 Epithelioid Sarcoma
    11014 t(X;5)(q13;q33) C 11551 Thrombocythemia
    11027 t(X;18)(p11.2;q11.2) C 11571 Bifocal Synovial Sarcoma
    11039 t(X;1)(q13.1;q11) C 11591 Ovarian Cancer
    11043 t (X;18) (q22.3;q23) C 11595 Isolated Growth Hormone Deficiency
    11050 t(X;1)(q26;p13.1) C 11606
    11058 t(X;9) (q13;p24) B 11650 Mental Retardation Syndrome
    11066 t(X;18)(p22;q23) C 11664 Acute Lymphoblastic Leukemia
    11159 t(X;17)(q27;q22) C 11799 Essential Thrombocythemia
    11163 t(X;2)(p11.2;q37) C 11802
    11171 t(X;15)(q28;p11.2) C 11812
    11192 t(X;11)(q24;q13) C 11871 Premature Ovarian Failure
    11205 t(X;9)(q12;p13.3) A 11886 Mental Retardation Syndrome
    11211 t(X;2)(q13;p23-24) C 11894 Leiomyosarcoma
    11218 t(X;11)(p11;q23) B 11906 Acute Myelocytic Leukemia-M2
    11219 t(X;11)(q24;q23) B 11907 Acute Myelocytic Leukemia
    11232 t(X;7)(p11.3;q11.21) C 11934
    11272 t(X;17)(q21.1;p13.1) A 11990
    11278 t(X;18)(q11.1;q11) A 12007
    11284 t(X;18)(p11.2;q11.2) C 12018 Synovial Sarcoma
    11286 t(X;5)(p11;q31.1) A 12021 Mental Retardation Syndrome
    11289 t(X;Y)(q13.1;q11.223) C 12025 Premature Ovarian Failure
    11291 t(X;1)(q28;q21) A 12032
    11297 t(X;13)(q13.3;p11.1) C 12043 Menkes Disease
    11299 t(X;2) (q22.3;p25.1) C 12045 Lissencephaly
    11302 t(X;9)(q13.2;p24) C 12050 Allan-Herndon-Dudley Syndrome
    11305 t(X;18)(p11.2;q11.2) C 12053 Synovial Sarcomas
    11308 t(X;8)(q22.1;q24.13) C 12059 Premature Ovarian Failure
    11335 t(X;20)(q10;q10) C 12108
    11336 t(X;20)(q10;q10) C 12109
    11363 t(X;20)(q13.1;q13.3) C 12144 Pancytopenia
    11364 t(X;20)(q13.1;q13.3) C 12145 Acute Myelocytic Leukemia
    11365 t(X;20)(q13;q12) C 12146 Myelodysplasia Syndrome
    11366 t(X;20)(q13;q13.3) C 12148 Myelodysplasia Syndrome
    11367 t(X;20)(q13;q13.3) C 12149 Acute Leukemia
    11368 t(X;20)(q13;q13.3) C 12150 Myelodysplasia Syndrome
    11369 t(X;20)(q13;q13.3) C 12150 Myelodysplasia Syndrome
    11370 t(X;20)(q13;q13.3) C 12154 Myelodysplasia Syndrome
    11396 t(X;9)(q12;p24) C 12197 Hypohidrotic Ectodermal Dysplasia
    11397 t(X;9)(q13.1;p24) C 12198 Hypohidrotic Ectodermal Dysplasia
    11408 t(X;18)(p11.2;q11.2) B 12217 Synovial Sarcoma
    11409 t(X;18)(p11.2;q11.2) B 12218 Synovial Sarcoma
    11410 t(X;18)(p11.2;q11.2) B 12219 Synovial Sarcoma
    11411 t(X;18)(p11.2;q11.2) B 12220 Synovial Sarcoma
    11412 t(X;18)(p11.2;q11.2) B 12221 Synovial Sarcoma
    11413 t(X;18)(p11.2;q11.2) A 12222 Synovial Sarcoma
    11414 t(X;18)(p11.2;q11.2) A 12223 Synovial Sarcoma
    11415 t(X;18)(p11.2;q11.2) A 12224 Synovial Sarcoma
    11416 t(X;18)(p11.2;q11.2) A 12225 Synovial Sarcoma
    11417 t(X;18)(p11.2;q11.2) A 12226 Synovial Sarcoma
    11421 t(X;17)(p11;q23) C 12231 Endometrial Stromal Sarcomas
    11422 t(X;8)(q28;q12) C 12233 Non-syndromic Mental Retardation
    11461 t(X;15)(q27.1;p11.2) C 12321 Hemophilia B
    11462 t(X;3)(p11;p11) C 12322 Tumor
    11468 der(16)t(X;16)(q13.1;p13) C 12340 Paraspinal Neuroblastoma
    11522 t(X;22)(p11.3;p11) C 12441
    11523 t(X;1)(q13.1;p36.3) C 12442 X-linked Anhidrotic Ectodermal Dysplasia
    11540 t(X;5)(p21.1;q31.1) A 12486 Duchenne Muscular Dystrophy
    11550 t(X;18)(p11.2;q11.2) B 12497 Synovial Sarcoma
    11551 t(X;18)(q11.22;q11.2) B 12498 Synovial Sarcoma
    11583 t(X;1)(p11;q21) C 12560 Human Papillary Renal Cell Carcinomas
    11595 t(X;1)(q21;p34) C 12577 Premature Ovarian Failure
    11617 t(X;10)(q22;p11) C 12609 Childhood Onset Type 2 Diabetes
    11626 t(X;18)(p11.21;q11.2) B 12618 Monophasic Fibrous
    11627 t(X;18)(p11;q11) B 12619 Monophasic Fibrous
    11628 t(X;18)(p11.2;q11.2) B 12624 Synovial Sarcoma
    11633 t(X;20)(p11.2;q13.3) B 12633 Synovial Sarcoma
    11663 t(X;3)(p22.1;p26.3) B 12667 Mental Retardation Syndrome
    11667 t(X;18)(p11.22;q11.2) B 12671 Synovial Sarcoma
    11668 t(X;9) (p22.3;q12) C 12672 Hypomagnesemia with Secondary Hypocalcemia (HSH)
    11707 t(X;2)(q22.3;p25) C 12737 Lissencephaly
    11711 t(X;18)(p11.2;q11.2) C 12746 Synovial Sarcoma
    11713 t(X;17)(p11;q25) B 12761 Alveolar Soft Part Sarcoma
    11714 t(X;17)(p11;q25) B 12762 Alveolar Soft Part Sarcoma
    11729 t(X;8)(p11.21;q11.21) C 12790 Aarskog Syndrome
    11738 t(X;18)(p11.2;q11.2) C 12805 Synovial Sarcoma
    11739 t(X;8)(p22.2;q23) A 12803
    11742 t(X;20)(q13;q13.3) C 12811 Myeloproliferative Disorder
    11744 t(X;9)(p22;q12) C 12816 Hypomagnesemia with Secondary Hypocalcemia
    11763 t(X;Y)(p22.2;q11.2) C 12855 Microphthalmia with Linear Skin Defects (MLS)
    11775 t(X;11)(q22;q23) C 12869 Acute Myelocytic Leukemia
    11812 t(X;9)(q13.1;p24) C 12922 Hypohidrotic Ectodermal Dysplasia
    11824 t(X, 9)(q11;q34) C 12932 Chronic Myeloid Leukemia
    11825 t(X;22)(q11;q11) C 12942 Chronic Myeloid Leukemia
    11842 t(X;9)(q13.1;p24) C 12963 X Linked Hypohidrotic Ectodermal Dysplasia
    11847 t(X;15)(q21;q23) C 12973 Primary Amenorrhea
    11887 t(X;13)(q21.2;p12) C 13040 Tapeto-choroidal Dystrophy
    11896 t(x;y)(p22.3;q11.2) C 13051 Hypoplastic, Irregular, Linear Skin Defects with A
    11897 t(x;y)(p22.3;q11.2) C 13052 bilateral microphthalmia with a left orbital cyst, linear skin
    11905 t(X;13)(q21.2;p12). C 13061 Mild Choroideremia
    11914 t(X;18)(p11.2;q11.2) C 13074 Synovial Sarcoma
    11920 t(X;4)(p21;q35) C 13081 Becker Muscular Dystrophy
    11924 t(X;3)(q25;q27) C 13086
    11938 t(X;12)(q22;p12) C 13118 Infertile
    11939 t(X;11)(q22;q13) C 13119
    11941 t(X;6)(p21;q21) C 13121 Duchenne Muscular Dystrophy
    11942 t(X;11)(q13;p15) C 13122 Idiopathic Acquired Sideroblastic Anemia
    11960 t(X;9) (p21;p22) C 13145 Duchenne Muscular Dystrophy
    11961 t(X;9)(q21;qter) C 13146 Amenorrhoea
    11981 t(X;Y)(p22;q11) B 13169 Turner Syndrome
    11982 t(X;Y)(p22;q11) B 13170 Turner Syndrome
    11983 t(X;Y)(p22;q11) B 13171 Turner Syndrome
    11987 t(X;9)(p11;q34) C 13175 Incontinentia Pigmenti
    11989 t(X;4)(q13;p16) C 13177
    12011 t(X;11)(q13;q23) A 13206 T-Cell Acute Lymphoblastic Leukemia
    12012 t(X;11)(q13.1;q23) A 13207 Acute Nonlymphoblastic Leukemia
    12018 t(X;10)(p11; p14) C 13213
    12031 t(X;5) (p21.2;q31.2) C 13226 Duchenne Muscular Dystrophy
    12036 t(X;2) (p21.2;q37) C 13231 Duchenne Muscular Dystrophy
    12052 t (X;15) (p21;q26) C 13271 Duchenne Muscular Dystrophy
    12054 t(X;21) (p21;p12) C 13273 Duchenne Muscular Dystrophy
    12066 t(X;20)(q26.1;q11.2) C 13288 Lowe Oculocerebrorenal Syndrome
    12067 t(X;2)(q13;q32.2) C 13289 Menkes Syndrome
    12071 t(X;15)(q25;q21) B 13298 Premature Ovarian Failure
    12072 t(X;20)(q24;q12) C 13299 Premature Ovarian Failure
    12073 t(X;17)(p11.4;p13.3) C 13300 Mental Retardation Syndrome
    12074 t(X;20)(p11.23;q13.3) C 13301 Mental Retardation Syndrome
    12094 t(X;18)(p11.2;q11.2) B 13330 Synovial Sarcoma
    12095 t(X;11)(q26;q23) B 13332 Premature Ovarian Failure