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
    10288 del(20)(p12p12) C 10428 Alagille Syndrome
    10615 del(20)(p11.23p12) C 10939 Alagille Syndrome
    10637 del(20)(p12.3p12.3) B 11041 Kindler Syndrome
    10810 del(20)(qterq13.33) C 11685
    10858 del(20)(p12.3p12.2) C 11851 Alagille Syndrome
    10925 del(20)(q11q13.3). C 12089 Chronic Myeloid Leukemia
    11186 del(20)(q11.2qter) C 13032 Leukemic
    10376 dup(20)(q13.1q13.3) C 12739
    10629 inv(20)(p12.2p13) B 11132 Alagille Syndrome
    10665 inv(20)(p13q13.3) C 11816
    10642 t(16;20)(q22;q13) C 10298 Acute Myelocytic Leukemia-M2
    10229 t(3;20)(q10;q10) C 10319 Small Cell Lung Cancer
    10296 t(3;20)(q13.3;p12.2) C 10427 Alagille Syndrome
    10398 t(4;20)(q12;p11.2) C 10577 Hepatocellular Carcinoma
    10400 t(7;20)(p15;q13.1) C 10579 Hepatocellular Carcinoma
    10402 t(14;20)(q21;q12) C 10581 Hepatocellular Carcinoma
    10434 t(1;20)(q11;q11.1) C 10631 Multiple Myeloma
    10524 t(12;20)(q13;p11.2) C 10780 Acute Nonlymphoblastic Leukemia
    10558 t(11;20)(p15;q11.2) A 10824 Acute Lymphoblastic Leukemia
    10559 t(11; 20) (p15;q11.2) A 10825 Myelodysplasia Syndrome
    10589 t(2;20)(p21;q11.2) C 10867 Nodular Goiter
    10619 t(16;20)(p12;p12) C 10925 Glioblastoma
    10628 t(2;20)(q21.3;p12) C 10940 Alagille Syndrome
    10705 t(13;20)(q11;q12) C 11076 B-Cell Acute Lymphoblastic Leukemia
    10790 t(3;20)(p14;p11) B 11214 Breast Tumor
    10979 t(5;20)(p15;q11) C 11501 Bladder Carcinoma
    11006 t(18;20)(q22.2;q13.3) C 11537 Mental Retardation Syndrome
    11135 t(17;20)(q12;q13) C 11771 Neuroblastoma
    11139 t(20;17)(q21;q13) C 11775 Neuroblastoma
    11277 t(18;20)(q21.1;q11.2) B 12006 Mental Retardation Syndrome
    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
    11526 t(20;22)(q13;q12) B 12458 Ewing Sarcoma
    11560 t(11;20)(q13.1;q13.13) C 12515 Asplenia Syndrome
    11581 der(11)t(11;20)(p15;q12) A 12557 T-Cell Myelodysplastic Syndrome
    11597 t(14;20)(q32.3;q13.1) C 12579 Non-Hodgkin Lymphoma
    11613 t(11;20)(p15;q11) A 12605 Acute Myelocytic Leukemia-M2
    11633 t(X;20)(p11.2;q13.3) B 12633 Synovial Sarcoma
    11726 t(2;20)(q21.3;p12) C 12782 Alagille Syndrome
    11742 t(X;20)(q13;q13.3) C 12811 Myeloproliferative Disorder
    11761 t(16;20)(p13;p11) C 12849 Acute Myeloid Leukemia
    11781 t(10;20)(p11;p13) C 12875
    12013 t(7;20)(q32.1;q13.2) C 13208 Smith-Lemli-Opitz Syndrome
    12066 t(X;20)(q26.1;q11.2) C 13288 Lowe Oculocerebrorenal Syndrome
    12072 t(X;20)(q24;q12) C 13299 Premature Ovarian Failure
    12074 t(X;20)(p11.23;q13.3) C 13301 Mental Retardation Syndrome