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Variant : CV382011 (GRCh37/hg19 11q13.2(chr11:67160949-67192950)x1) Homo sapiens

Symbol: CV382011
Name: GRCh37/hg19 11q13.2(chr11:67160949-67192950)x1
Condition: See cases [RCV000446214]
Clinical Significance: likely benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: CARNS1   PPP1CA   RAD9A   TBC1D10C  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371167,160,949 - 67,192,950CLINVAR
Cytogenetic Map1111q13.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12850941
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-10-20
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.