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Variant : CV154508 (GRCh38/hg38 2q37.3(chr2:241481406-242126245)x1) Homo sapiens

Symbol: CV154508
Name: GRCh38/hg38 2q37.3(chr2:241481406-242126245)x1
Condition: See cases [RCV000134170]
Clinical Significance: uncertain significance
Last Evaluated: 08/19/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ATG4B   BOK   BOK-AS1   D2HGDH   DTYMK   FAM240C   FARP2   GAL3ST2   ING5   LINC01237   LINC01238   LINC01880   LINC01881   LOC285097   NEU4   PDCD1   RTP5   STK25   THAP4  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000002.12:g.(?_241481406)_(242126245_?)del
NC_000002.11:g.(?_242420821)_(243059659_?)del
NC_000002.10:g.(?_242069494)_(242717069_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh382241,481,406 - 242,126,245CLINVAR
GRCh372242,420,821 - 243,059,659 (+)CLINVAR
Build 362242,069,494 - 242,717,069CLINVAR
Cytogenetic Map22q37.3CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9481750
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-05-26
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.