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Variant : CV605873 (GRCh37/hg19 15q11.2(chr15:21341905-22595580)x3) Homo sapiens

Symbol: CV605873
Name: GRCh37/hg19 15q11.2(chr15:21341905-22595580)x3
Condition: not provided [RCV000751173]
Clinical Significance: benign
Last Evaluated: 07/02/2012
Review Status: no assertion criteria provided
Related Genes: OR4M2   OR4N4   POTEB  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371521,341,905 - 22,595,580CLINVAR
Cytogenetic Map1515q11.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14366499
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.