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Variant : CV605422 (GRCh37/hg19 13q14.3(chr13:52506048-52778214)x1) Homo sapiens

Symbol: CV605422
Name: GRCh37/hg19 13q14.3(chr13:52506048-52778214)x1
Condition: not provided [RCV000750722]
Clinical Significance: likely benign
Last Evaluated: 06/03/2016
Review Status: no assertion criteria provided
Related Genes: ALG11   ATP7B   NEK3   NEK5   UTP14C  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371352,506,048 - 52,778,214CLINVAR
Cytogenetic Map1313q14.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14366048
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-07
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.