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
    10036 del(16)(p11.2pter) C 10147
    10054 del(16)(p13p13) C 10296 Acute Myelocytic Leukemia-M2
    10318 del(16)(q22.2q22.2) A 10492 Anaphylactic Shock
    10325 del(16)(q22qter) C 10518 Wilms Tumour
    10327 del(16)(q22q22) C 10555 Acute Myelocytic Leukemia-M4
    10346 del(16)(p13.3p13.3) C 10627 Rubinstein-Taybi Syndrome
    10631 del(16)(q23.1q24.2) C 10970
    10663 del(16)(qterq22) C 11112
    10744 del(16)(p12.1p12.1) B 11439 Batten Disease
    10770 del(16)(q24.3q24.3) A 11601 Hereditary Spastic Paraplegia
    10788 del(16)(pterp11.2) C 11632 Autism
    10789 del(16) (p13.3p13.3) C 11635 Mental Retardation Syndrome
    10811 del(16)(p13.3p13.3) B 11691 Thalassaemia
    10812 del(16)(p13.3p13.3) B 11693 Thalassaemia
    10813 del(16)(p13.3p13.3) B 11695 Thalassaemia
    10814 del(16)(p13.3p13.3) B 11697 Thalassaemia
    10815 del(16)(p13.3p13.3) B 11700 Thalassaemia
    10837 del(16)(p13.3p13.3) A 11813 Thalassemia
    10838 del(16)(p13.3p13.3) A 11814 Thalassemia
    10839 del(16)(p13.3p13.3) A 11815 Thalassemia
    10930 del(16)(p11.2p12.2) C 12102
    11022 del(16)(p11.2p12.2) C 12422 Developmental Delay
    11026 del(16)(p13.3p13.3) A 12450 Mucolipidosis III Gamma
    11027 del(16)(p13.3p13.3) A 12451 Mucolipidosis III Gamma
    11103 del(16)(p13.3p13.3) A 12741
    11105 del(16)(p13.3p13.3) A 12750 Tuberous Sclerosis (TSC)
    11106 del(16)(p13.3p13.3) A 12751 Tuberous Sclerosis (TSC)
    11107 del(16)(p13.3p13.3) A 12752 Tuberous Sclerosis (TSC)
    11108 del(16)(p13.3p13.3) A 12753 Tuberous Sclerosis (TSC)
    11129 del(16)(p13.3p13.3) A 12815 Alpha Thalassemia
    11151 del(16)(q22qter) C 12900 Tumor
    11237 del(16)(q22qter) C 13268
    11240 del(16)(p13.3p13.3) A 13291
    10237 dup(16)(q22.2q22.2) B 10493 Anaphylactic Shock
    10294 dup(16)(p13.11p13.2) C 11624
    10297 dup(16)(q22.1q22.1) C 11628 Autism
    10380 dup(16)(p13.3p13.3) A 12815 Alpha Thalassemia
    10017 ins(16)(p11.2) A 10982 Adrenoleukodystrophy
    10037 ins(16;2) (q22.1;p16.1p16.3) C 11645 Atrial Septal Defect
    10008 inv(l6)(p13q22) C 10128 Acute Myelocytic Leukemia
    10015 inv(16)(p13q22) C 10298 Acute Myelocytic Leukemia-M2
    10016 inv(16)(p13q22) C 10300 Acute Myelocytic Leukemia-M4
    10025 inv(16)(p13q22) C 10554 Acute Myelocytic Leukemia-M4
    10051 inv(16)(p13q22) C 10892 Acute Myelocytic Leukemia-M4
    10622 inv(16)(p13.3p12.1) C 11027 Mental Retardation Syndrome
    10623 inv(16) (P13q22) C 11070 Acute Myelocytic Leukemia
    10649 inv(16)(p13q22) B 11532 T-Cell Myelodysplastic Syndrome
    10657 inv(16)(p13q22) A 11660 Acute Myelocytic Leukemia
    10683 inv(16)(p13q22) C 12038 Acute Myelocytic Leukemia
    10737 inv(16)(p13q22) C 12802 Acute Myelomonocytic Leukemia M4Eo
    10738 inv(16)(p13q22) C 12810 Acute Myelocytic Leukemia
    10739 inv(16)(p13q22) C 12828 Acute Myelocytic Leukemia
    10740 inv(16)(p13q22) C 12843 Acute Myeloid Leukemias
    10755 inv(16)(p13q22) C 13193 Acute Myeloid Leukemia
    10760 Inv(16)(p13q22) C 13274 Acute Nonlymphocytic Leukemia
    10077 t(2;16)(p13;p13) B 10116 Acute Nonlymphoblastic Leukemia
    10078 t(7;16)(q34;p13.3) C 10116 Acute Nonlymphoblastic Leukemia
    10079 t(8;16)(p11;p13) C 10117 Acute Nonlymphocytic Leukemia
    10087 t(16;16)(p13;q22) C 10129 Acute Myelocytic Leukemia
    10104 t(12;16)(p13.1 ;p11.2) C 10147
    10108 t(9;16)(p21.2;13.3) C 10152
    10109 t(9;16)(p21.2;p13.3) C 10153
    10110 t(2;16)(q37.1;q24.3) C 10154
    10201 t(12;16)(q32;q16) B 10274 Lipoma
    10641 t(16;9)(q22, p24) C 10296 Acute Myelocytic Leukemia-M2
    10642 t(16;20)(q22;q13) C 10298 Acute Myelocytic Leukemia-M2
    10643 t(16;1)(q22;p32) C 10300 Acute Myelocytic Leukemia-M4
    10238 t(15;16)(q12;p13) C 10333 Dysplastic Nevus
    10240 t(16;21)(p11.2;q22) B 10334 Acute Myelocytic Leukemia-M4
    10286 t(8;16)(q24.3;p13.3) C 10410 Polycystic Kidney Disease
    10317 t(12;16)(q13;p11) C 10467 Myxoid Liposarcoma
    10361 t(Y;16)(q12;q24.3) C 10531 Lymphedema-distichiasis
    10403 t(16;22)(q13;q11.2) C 10582 Hepatocellular Carcinoma
    12080 t(2;16)(q37.3;q24.3) C 13310
    12107 t(5;16)( ;q21.1) C 10610 Townes-Brocks Syndrome
    10423 t(11;16)(q14;p13) C 10615 Hepatocellular Carcinoma
    10480 t(5;16)(p15.3;q23.2) B 10696
    10575 t(7;16)(q11.23;q21) A 10847 Williams-Beuren Syndrome
    10606 t(2;16)(q33;q24) C 10903 Nodular Tenosynovitis
    10607 t(5;16)(q11;q24) C 10904 Nodular Tenosynovitis
    10619 t(16;20)(p12;p12) C 10925 Glioblastoma
    10678 t(14;16)(p32;p13.3) C 11027 Mental Retardation Syndrome
    10689 t(3;16)(q23;p13) C 11039 Acute Lymphoblastic Leukemia
    10720 t(1;16)(q12;p13.3) C 11096 Mental Retardation Syndrome
    10721 t(14;16)(q32;p13.3) C 11097 Mental Retardation Syndrome
    10761 t(8;16)(p11;p13) A 11181 Acute Myelocytic Leukemia-M5
    10762 t(8;16)(p11;p13) A 11182 Acute Myelocytic Leukemia-M5
    10764 t(8;16)(p11;p13) A 11184 Acute Myelocytic Leukemia-M4
    10765 t(8;16)(p11;p13) A 11185 T-Cell Acute Myelocytic Leukemia-M5
    10800 t(8;16)(p11;p13) B 11229 Acute Myelocytic Leukemia
    10801 t(8;16)(p11;p13) B 11230 Bilateral Ovarian Dysgerminoma
    10802 t(8;16)(p11;p13) B 11231 Acute Myelocytic Leukemia
    10803 t(8;16)(p11;p13) B 11232 Common-Acute Lymphoblastic Leukemia
    10807 t(16;19)(q13.1;p13) C 11237 Hepatocellular Carcinoma
    10844 t(16;18)(p13;q21.3) C 11289 Follicular Lymphoma
    10888 t(16;17)(q22;p13) C 11364 Aneurysmal Bone Cysts
    10890 t(16;17)(q22;p13) C 11367 Aneurysmal Bone Cysts
    10903 t(11;16)(q23;p13) A 11381 T-Cell Acute Lymphoblastic Leukemia
    10904 t(11;16)(q23;p13) A 11382 T-Cell Chronic Myelomonocytic Leukemia
    10905 t(11;16)(q23;p13) A 11383 T-Cell Acute Myelocytic Leukemia-M5
    10906 t(11;16)(q23;p13) A 11384 T-Cell Myelodysplastic Syndrome
    10907 t(11;16)(q23;p13) A 11385 T-Cell Acute Myelocytic Leukemia-M5
    10908 t(11;16)(q23;p13) A 11386 T-Cell Acute Myelocytic Leukemia-M4
    10919 t(X;16)(q21.2;p12) C 11399 Premature Ovarian Failure
    10987 t(7;16)(p15;q22) C 11511
    10988 t(8;16)(q22.1;q13) C 11512
    10990 t(16;18)(q24;q21.1) C 11514
    11029 t(4;16)(q26;q22) C 11574
    11077 t(2;16)(q35;p11) C 11686 Ewing Sarcoma
    11123 t(16;17)(q22;q21) C 11758 Neuroblastoma
    11138 t(16;17)(q22;q12) C 11774 Neuroblastoma
    11162 t(16;17)(q24;q11) C 11803
    11190 t(11;16)(p13;q24.3) C 11868 Silver-Russel Syndrome
    11209 t(10;16)(q11;q13) C 11890 Leiomyosarcoma
    11215 t(7;16)(p22.1;p11.2) B 11903 Autism
    11239 t(16;22)(p13.3;q11.2) C 11944 Congenital Cataract
    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
    11317 t(3;16)(q27.3;p12.1) A 12078 Diffuse Large Cell Lymphoma
    11353 t(6;16)(p21.1;q22.2) C 12132 Prostatic Adenocarcinoma
    11418 t(16;22)(p13.3;q11.2-12) C 12227 Primitive Neuroectodermal Tumor
    11435 t(12;16)(q13;p11) C 12261 Myxoid and Round Cell Liposarcoma
    11468 der(16)t(X;16)(q13.1;p13) C 12340 Paraspinal Neuroblastoma
    11485 t(1;16)(q10;p10) C 12370 Multiple Myeloma
    11487 t(1;16)(q10;p13) C 12372 Multiple Myeloma
    11518 t(15;16)(q15;p13) C 12435 Lymphoproliferative Disorders
    11549 t(12;16)(q13;p11) C 12496 Lipoblastoma
    11554 t(9;16)(q22;q11) C 12502 Malignant Fibrous Histiocytomas
    11567 t(16;18)(q10;p10) C 12522 Malignant Fibrous Histiocytomas
    11593 t(16;21)(p11;q22) C 12574 Acute Myelocytic Leukemia
    11602 t(5;16)(q31;p11.2) C 12584 Anemia with Ring Sideroblasts
    11625 t(3;16)(p21;q24) C 12617 Dupuytren Contracture
    11631 t(3;16)(q27;p13.3) C 12631 Follicular Lymphoma
    11704 t(8;16)(p11.21;p13.3) A 12733 Acute Myelocytic Leukemia
    11750 t(16;16)(p13;q22) C 12829 Acute Myelocytic Leukemia
    11751 t(11;16)(q23;p13) B 12830 Acute Myelocytic Leukemia-M2
    11752 t(11;16)(q23;p13.3) B 12831 Breast Cancer
    11753 t(11;16)(q23;p13.3) B 12833 Acute Lymphoblastic Leukemias
    11754 t(11;16)(q23;p13) B 12834 Mantle Cell Lymphoma
    11755 t(11;16)(q23;p13.3) B 12835 Mantle Cell Lymphoma
    11756 t(11;16)(q23;p13) B 12837 Neuroblastoma
    11761 t(16;20)(p13;p11) C 12849 Acute Myeloid Leukemia
    11784 t(16;21)(q24;q22) B 12882 Acute Myeloblastic Leukemia
    11788 t(14;16)(q32;q23) B 12886 B-Cell Tumors
    11797 t(12;16)(q13;p11) C 12897 Tumor
    11861 t(12;16)(q13.3;p11.2) A 12994 Myxoid Liposarcoma
    11883 t(12;16)(q13;p11) C 13036 Tumor
    11886 t(8;16)(p11;p13) C 13039 Acute Nonlymphocytic Leukemia
    11911 t(16;1)(p36.3;p13.3) C 13070 Autosomal Dominant Polycystic Kidney Disease
    11928 t(12;16)(q13;p11) C 13101 Tumor
    11975 t(8;16)(p11;p13) C 13163 Acute Nonlymphocytic Leukemia
    11998 t(4;16)(q26;q22) C 13187 Rieger Syndrome
    12040 t(2;16)(q33;q24) C 13238
    12055 t(12;16)(q13;p11) C 13275 Tumor
    12212 t(16;21)(q13;q22.3) B 13511 Prostate Cancer