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Variant : CV382803 (GRCh37/hg19 20p12.1(chr20:16672584-17288277)x3) Homo sapiens

Symbol: CV382803
Name: GRCh37/hg19 20p12.1(chr20:16672584-17288277)x3
Condition: See cases [RCV000448689]
Clinical Significance: likely benign
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: OTOR   PCSK2   SNRPB2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372016,672,584 - 17,288,277CLINVAR
Cytogenetic Map2020p12.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 12853393
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-06-23
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.