Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

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)
Evidence: clinical testing
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


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.