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Variant : CV593347 (GRCh37/hg19 15q11.2(chr15:22287223-22590179)x3) Homo sapiens

Symbol: CV593347
Name: GRCh37/hg19 15q11.2(chr15:22287223-22590179)x3
Condition: not provided [RCV000738647]
Clinical Significance: benign
Last Evaluated: 03/07/2012
Review Status: no assertion criteria provided
Related Genes: OR4M2   OR4N4  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371522,287,223 - 22,590,179CLINVAR
Cytogenetic Map1515q11.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14354027
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-11-12
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.