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
    10343 del(Y)(q11) C 10620
    10357 del(Y)(qterq11.21) C 10680
    10774 del(x)(q28q28) A 11607 Rett Syndrome
    10820 del(Y)(qterq11.2) C 11718
    11102 del(11)(q11.23qter) C 12742 Intracytoplasmic Sperm Injection
    11180 del(Y)(q11.2qter) C 13016 Steroid Sulphatase
    10251 dup(Y)(p11.32;p11.32pter) C 11094 Azoospermia
    10641 inv(Y)(p11.31q12) C 11282 Gonadoblastoma
    10761 inv(Y)(p11q11) C 13294
    10006 r(Y)(p11q11) C 11477
    10007 r(Y)(p11q11) C 11478
    10010 r(Y)(p11q11) C 11901 Azoospermia
    10045 t(X;Y)(q22;p11) C 10069
    10273 t(X;Y)(p22.3;q11.2) C 10387
    10361 t(Y;16)(q12;q24.3) C 10531 Lymphedema-distichiasis
    10378 t(Y;14)(q12;p11) C 10548 Infertility
    10406 t(Y;17)(q11.2;q22) C 10585 Hepatocellular Carcinoma
    10548 t(Y;1)(q12;q12) C 10810 Polycythemia Vera
    10608 t(Y;22)(p11;q11) C 10905 Chronic Myeloid Leukemia
    10632 t(X;Y)(p22.3;q11.2) C 10944
    10634 t(X;Y)(q28;q11.21) C 10946
    10741 t(Y;7)(p11.32;p15.3) C 11129
    10860 t(Y;4)(q11.2;q21) C 11323 Epileptic Encephalopathy
    10887 t(Y;17)(q11.2;q24.3) C 11363 Acampomelic Form of Campomelic Dysplasia
    11012 t(Y;8)(q11.23;p23.1) C 11549
    11034 t(Y;15)(p11.2;q12) B 11578
    11289 t(X;Y)(q13.1;q11.223) C 12025 Premature Ovarian Failure
    11292 der(Y)t(Y;1)(q12;q25) B 12033 Kabuki Syndrome,acute Myeloid Leukemia
    11496 t(Y;6)(q12;p11.1) C 12400 Infertility
    11620 t(Y;5)(q11.2;q33) C 12612 Dupuytren Contracture
    11622 t(Y;14)(q12;q24) C 12614 Dupuytren Contracture
    11763 t(X;Y)(p22.2;q11.2) C 12855 Microphthalmia with Linear Skin Defects (MLS)
    11803 t(y;4)(p11;q32) C 12907 Azoospermia
    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
    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