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Variant : CV675548 (GRCh37/hg19 20p12.1(chr20:16688627-17288943)x3) Homo sapiens

Symbol: CV675548
Name: GRCh37/hg19 20p12.1(chr20:16688627-17288943)x3
Condition: not provided [RCV000848647]
Clinical Significance: uncertain significance
Last Evaluated: 10/18/2017
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
GRCh372016,688,627 - 17,288,943CLINVAR
Cytogenetic Map2020p12.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14980192
Created: 2019-10-08
Species: Homo sapiens
Last Modified: 2020-07-07
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.