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
    10051 del(4)(p16.1pter) C 10285 Wolf-Hirschhorn Syndrome
    10057 del(4)(p16.3pter) B 10327 Wolf-Hirschhorn Syndrome
    10333 del(4)(p10pter) C 10576 Hepatocellular Carcinoma
    10379 del(4)(q13q31) C 10760 Acute Myelocytic Leukemia
    10640 del(4)(p11p15.1) C 11045 Chronic Lymphoblastic Leukemia
    10703 del(4) (p16pter) C 11278 Wolf-Hirschhorn Syndrome
    10751 del(4)(qterq35) C 11529
    10758 del(4)(p15.33p16.3) C 11560
    10798 del(4)(q28.3q31.22) C 11653 Primary Hypogonadism
    10816 del(4)(q12q12) A 11707 Chronic Eosinophilic Leukemia
    10835 del(4)(q25q25) C 11808 Axenfeld-Rieger Syndrome
    10836 del(4)(q25q25) C 11806 Polycythemia Vera
    10876 del(4)(p16.3p16.3) C 11902 Wolf-Hirschhorn Syndrome
    10880 del(4)(p14pter) C 11936 Wolf-Hirschhorn Syndrome
    10912 del(4)(q13.3q21.1) A 12057 Developmental Delay
    10915 del(4)(q32.1q32.1) A 12063 Macrocephaly
    10916 del(4)(q21.23q21.23) A 12065 Developmental Delay, Learning Difficulties
    10918 del(4)(q13.3q13.3) A 12065 Developmental Delay, Learning Difficulties
    11112 del(4)(p16.3p16.3) B 12758 Wolf-Hirschhorn Syndrome (WHS)
    11137 del(4)(p16.3pter) C 12842 Wolf-Hirschhorn Syndrome
    11152 del(4)(q34.3q34.3) A 12906 Aspartylglucosaminuria
    11207 del(4)(q31qter) C 13117 Multiple Congenital Anomalies
    11209 del(4)(q33qter) C 13124
    11241 del(4)(q25q27) C 13302 Rieger Syndrome
    10230 dup(4)(q21;q21q21) A 10340 Acute Lymphocytic Leukemia
    10231 dup(4)(q21;q21q21) A 10339 Acute Lymphocytic Leukemia
    10245 dup(4)(q35) C 10860 Facio-scapulo-humeral Type Muscular Dystrophy
    10374 dup(4)(q24q35) C 12635
    10688 inv(4)(p13q21) A 12212 Cleft Lip
    10046 inv(4)(q21q32) C 10835
    10626 inv(4)(p12p15.3) B 11111 Autism
    10661 inv(4)(q13q25) C 11683 Schizophrenia
    10008 r(4)(p16q35) B 11524
    11378 t(4;8)(p14;q12) C 12176 Pleomorphic Adenomas
    10075 t(4;11)(q21;q23) C 10113 Acute Lymphoblastic Leukemia
    10092 t(4;11)(q21;q23) C 10136 Acute Lymphoblastic Leukemia
    10122 t(4;11)(q21;q23) C 10166 Acute Lymphoblastic Leukemia
    10145 t(4;11)(q21;q23.3) C 10191 Acute Lymphoblastic Leukemia
    10149 t(4;13)(q26;q12) C 10197 Myofascial Pain Dysfunction Syndrome
    10152 t(4;11)(q21.3;q25) C 10200 Psoriasis
    10159 t(4;13)(q21;q22) C 10211
    10160 t(4;13)(p14;q32) C 10212
    10177 t(3;4)(q23;p15.2) B 10234 Infertility
    10203 t(3;4)(q23;p15.2) C 10278 Blepharophimosis Syndrome
    10180 t(4;14)(p16;q32.3) B 10239 Chronic Myeloid Leukemia
    11675 t(4;11)(q23;q23) C 12683 Acute Myelocytic Leukemia
    10241 t(4;11)(q23;p15) A 10337 T-Cell Acute Lymphoblastic Leukemia
    10242 t(4;11)(q23;p15) A 10338 T-Cell Acute Lymphoblastic Leukemia
    10243 t(4;11)(q21;q23) A 10339 Acute Lymphocytic Leukemia
    10244 t(4;11)(q21;q23) A 10340 Acute Lymphocytic Leukemia
    10249 t(4;13)(q25;q12) C 10353 Myofascial Pain Dysfunction Syndrome
    10263 t(4;11)(q21;q23) B 10374 Acute Lymphoblastic Leukemia
    10264 t(4;11)(q21;q23) B 10375 Acute Lymphoblastic Leukemia
    10265 t(4;11)(q21;q23) B 10376 Acute Lymphoblastic Leukemia
    10266 t(4;11)(q21;q23) B 10377 Acute Lymphoblastic Leukemia
    10267 t(4;11)(q21;q23) B 10378 Acute Lymphoblastic Leukemia
    10268 t(4;11)(q21;q23) B 10379 Acute Lymphoblastic Leukemia
    12085 t(4;9)(q13;p32) C 13316 Solitary Fibrous Tumor
    10280 t(4;11)(q21;q23) A 10395 Acute Lymphoblastic Leukemia
    10281 t(4;11)(q24.21;q23) B 10404 Acute Lymphoblastic Leukemia
    10323 t(2;4)(p24.3;q34.3) C 10476 Neuroblastoma
    11372 t(4;11)(p16.2;p15.4) C 12165
    10345 t(4;14)(q21;p12) C 10509
    10352 t(4;11)(q22.1;q23.3) A 10521 Acute Lymphoblastic Leukemia
    10353 t(4;11)(q21.3;q23.3) A 10522 Acute Lymphoblastic Leukemia
    10398 t(4;20)(q12;p11.2) C 10577 Hepatocellular Carcinoma
    10461 t(4;14)(q12;q11.2) C 10661 Aggressive NK Cell Leukemia
    10463 t(4;13)(q25;p11.2) C 10663 Aggressive NK Cell Leukemia
    10555 t(4;11)(q21;q23) C 10821 Malignant Lymphoma
    10566 t(4;7)(q31.1;q21.3) C 10837
    12088 t(4;11)(q10;q13) C 13320 Hepatocellular Carcinoma
    10586 t(4;21)(q31;q22) B 10859 T-Cell Acute Lymphoblastic Leukemia
    10591 t(X ;4(q21.2;p16.3) C 10873
    10593 t(1;4)(q12;p16) C 10875 Non-Hodgkin Lymphoma
    10603 t(4;11)(p16.3;p15.5) C 10893 Wolf-Hirschhorn Syndrome
    10640 t(4;11)(q32;q23) C 10969
    10699 t(2;4)(p22;q31.1) C 11065 Neuroblastoma
    10719 t(4;13)(p16.1;q21.31) C 11095 Schizophrenia
    10728 t(4;6)(p15;q23) C 11110 Nonkeratinizing Squamous Cell Carcinoma
    10819 t(4;8)(p15.3;q24.1) B 11253 Oculo-auriculo-vertebral Spectrum
    10831 t(2;4)(p21;q25) C 11268 Anaplastic Large Cell Lymphoma
    10840 t(4;12)(q31;q21) C 11279 Myelodysplasia Syndrome
    10845 t(4;14)(p16;q32) A 11290 Myeloma
    10860 t(Y;4)(q11.2;q21) C 11323 Epileptic Encephalopathy
    10871 t(4;11)(p14;q25) C 11338
    10913 t(X;4)(q21;q31.3) C 11393 Premature Ovarian Failure
    10924 t(X;4)(q24;q35) C 11404 Premature Ovarian Failure
    10935 t(4;11)(q21;q23) C 11435 Acute Lymphoblastic Leukemia
    10945 t(4;12)(q11;p13) B 11449 Acute Myelocytic Leukemia-M0
    11007 t(3;4)(p26;p16) C 11538 Mental Retardation Syndrome
    11017 t(4;5)(q13.1;p15.33) A 11556 Mental Retardation Syndrome
    11018 t (X;14) (q27.1;q32.3) C 11558 Hemophilia B
    11023 t(1;4)(q31;p15.1) B 11564
    11028 t(4;11)(q27;q21) C 11573
    11029 t(4;16)(q26;q22) C 11574
    11037 t(4;5)(q21;q33) B 11589 Myofascial Pain Dysfunction Syndrome
    11044 t(4;21)(p16;q21) C 11597 Cleidocranial Dysplasia
    11045 t(4;6)(p16;p21.1) C 11598 Cleidocranial Dysplasia
    11052 t(4;5)(q21.1;q31.3) B 11633 Familial Polycystic Kidney Disease
    11067 t(4;11)(q21;q23) C 11665 Acute Lymphoblastic Leukemia
    11094 t(4;11)(q27;q13) B 11712 Acute Lymphoblastic Leukemia
    11115 t(4;6)(q12;p23) C 11748
    11129 t(4;17)(q32;q21) C 11765 Neuroblastoma
    11140 t(14;17)(q11;p12) C 11776 Neuroblastoma
    11155 t(4;21)(q28;q22.3) A 11793 Acute Lymphoblastic Leukemia
    11156 t(4;21)(q28;q22.3) A 11793 Acute Lymphoblastic Leukemia
    11157 t(4;11)(p12;q23) A 11796 Neuroblastoma
    11158 t(4;11)(q22.1;q23.3) A 11798 Acute Myelocytic Leukemia
    11161 t(4;17)(p15;q22) C 11801 Chronic Myeloid Leukemia
    11167 t(4;17)(q25;q22) C 11808 Axenfeld-Rieger Syndrome
    11235 t(3;4)(q27.3;q32.3) C 11938 Omphalocele
    11271 t(3;4)(q21.3;q31.3) A 11989 Renal Cell Cancer
    11274 t(4;16)(q35.2;q23.2) B 11996 Apraxia of Speech
    11275 t(4;16)(q35.2;q23.2) B 11997 Apraxia of Speech
    11276 t(4;16)(q35.2;q23.2) B 11998 Apraxia of Speech
    11307 t(4;8)(q21.1;p12) C 12057 Developmental Delay
    11321 t(4;22)(q12;q11) A 12087 Chronic Myeloproliferative Disease
    11320 t(4;22)(q12;q11) A 12084 Chronic Myeloproliferative Disease
    11327 t(1;4)(p36;q35.2) A 12093
    11328 t(4;22)(q12;q11) B 12096 Chronic Myeloid Leukemia
    11373 t(4;11)(p16.2;p15.4) C 12166
    11407 t(4;14)(q25;q13) B 12215
    11456 t(1;4)(q21;q35) C 12308 Lymphoplasmacytic Lymphoma
    11470 t(4;9)(q35;q12) C 12342 Cardiac Myxoma
    11482 t(1;4)(q11;q35) C 12365 Multiple Myeloma
    11519 t(4;12)(q27;q15) C 12436 Fibroadenoma
    11534 t(3;4)(q27;p11) C 12480 Diffuse Large B-Cell Lymphomas
    11580 t(4;11)(q21;q23.3) A 12556 Acute Lymphoblastic Leukemia
    11565 t(1;4)(p32;q33) C 12520 Malignant Fibrous Histiocytomas
    11601 t(4;11)(q21;q23) C 12583 Acute Leukemia
    11604 t(4;11)(q22.1;q23.3) A 12585 Aggressive Mixed-lineage Leukemia
    11615 t(4;18)(q35.1;q22.3) C 12607
    11712 t(4;7)(p15.31;q36.1) A 12747 T-Cell Acute Lymphoblastic Leukemia
    11745 t(4;13)(q12;q14) B 12818 Bilateral Retinoblastom
    11748 t(4;11)(q21;p15.5) C 12824 T-Cell Acute Lymphoblastic Leukemia
    11769 t(4;11)(q21;q23) C 12863 Acute Lymphoblastic Leukemia
    11803 t(y;4)(p11;q32) C 12907 Azoospermia
    11811 t(4;11)(q32;q23) C 12921 Acute Lymphoblastic Leukemia
    11863 t(4;17)(q28.3;q24.3) A 12997 Campomelic Dysplasia
    11900 t(4;11 )(q21.3; q23.1) C 13055 Non-Hodgkin Lymphoma
    11917 t(4;14)(q21;q32) C 13077 Acute Leukemia
    11920 t(X;4)(p21;q35) C 13081 Becker Muscular Dystrophy
    11930 t(4;11)(q21;q23) C 13103 Acute Lymphocytic Leukemia
    11936 t(4;9)(q35;q12) C 13115
    11943 t(4;11)(q22;p13) C 13125 Wilms Tumor
    11968 t(4;8)(p15.3;p22) C 13154 Familial Wolf Syndrome
    11989 t(X;4)(q13;p16) C 13177
    11997 t(4;11)(q27;q21) C 13186 Rieger Syndrome
    11998 t(4;16)(q26;q22) C 13187 Rieger Syndrome
    12009 t(4;21) (p16;q22) C 13203 Chronic Myeloid Leukemia
    12015 t(4;22)(p14;q11) C 13210 Acute Myelocytic Leukemia
    12016 t(4;9)(p14;q34) C 13210 Acute Myelocytic Leukemia
    12035 t(4;11)(q12;q23) C 13230 Acute Myelogenous Leukemia
    12057 t(4;11)(q21;q23) C 13277 Acute Leukemia
    12059 t(4;11)(q21;q23) C 13280 Leukemic
    12076 t(4;12)(q25;q15) C 13303 Rieger Syndrome
    12096 t(4;5)(q21;q22) C 13333 Acute Promyelocytic Leukemia
    10016 t(4;7;8;17)(p15.1;p15.3;q12.1;q25.1) B 12999 Campomelic Dysplasia
    10012 t(4;15)(q35.2qter;q14q14) C 11380 Prader-Willi Syndrome