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

Variant : CV605868 (GRCh37/hg19 15q11.2(chr15:20845014-21200585)x3) Homo sapiens

Symbol: CV605868
Name: GRCh37/hg19 15q11.2(chr15:20845014-21200585)x3
Condition: not provided [RCV000751168]
Clinical Significance: benign
Last Evaluated: 03/07/2012
Review Status: no assertion criteria provided
Related Genes: POTEB2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371520,845,014 - 21,200,585CLINVAR
Cytogenetic Map1515q11.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14366494
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2019-10-15
Status: ACTIVE



NHLBI Logo

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