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Variant : CV605558 (GRCh37/hg19 13q32.1(chr13:95253291-95258830)x1) Homo sapiens

Symbol: CV605558
Name: GRCh37/hg19 13q32.1(chr13:95253291-95258830)x1
Condition: not provided [RCV000750858]
Clinical Significance: benign
Last Evaluated: 12/31/2011
Review Status: no assertion criteria provided
Related Genes: GPR180  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371395,253,291 - 95,258,830CLINVAR
Cytogenetic Map1313q32.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14366184
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-21
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.