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Variant : CV592629 (GRCh37/hg19 12q15(chr12:69862184-69864170)x1) Homo sapiens

Symbol: CV592629
Name: GRCh37/hg19 12q15(chr12:69862184-69864170)x1
Condition: not provided [RCV000737929]
Clinical Significance: benign
Last Evaluated: 10/26/2011
Review Status: no assertion criteria provided
Related Genes: FRS2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371269,862,184 - 69,864,170CLINVAR
Cytogenetic Map1212q15CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14353304
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-12-03
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.