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Variant : CV157471 (GRCh38/hg38 11q13.2(chr11:67397196-67644438)x1) Homo sapiens

Symbol: CV157471
Name: GRCh38/hg38 11q13.2(chr11:67397196-67644438)x1
Condition: See cases [RCV000136875]
Clinical Significance: benign
Last Evaluated: 01/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ACY3   AIP   C11orf72   CABP2   CABP4   CARNS1   CDK2AP2   CORO1B   GPR152   GSTP1   MIR6752   NDUFV1   NUDT8   PITPNM1   PPP1CA   PTPRCAP   RAD9A   RPS6KB2   TBC1D10C   TBX10   TMEM134  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_67397196)_(67644438_?)del
NC_000011.9:g.(?_67164667)_(67411909_?)del
NC_000011.8:g.(?_66921243)_(67168485_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh381167,397,196 - 67,644,438CLINVAR
GRCh371167,164,667 - 67,411,909CLINVAR
Build 361166,921,243 - 67,168,485CLINVAR
Cytogenetic Map1111q13.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9484436
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-10-15
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.