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Variant : CV603185 (GRCh37/hg19 9q21.2(chr9:80185929-80207402)x1) Homo sapiens

Symbol: CV603185
Name: GRCh37/hg19 9q21.2(chr9:80185929-80207402)x1
Condition: not provided [RCV000748485]
Clinical Significance: benign
Last Evaluated: 12/09/2015
Review Status: no assertion criteria provided
Related Genes: GNA14  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh37980,185,929 - 80,207,402CLINVAR
Cytogenetic Map99q21.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14363818
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-01-14
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.