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

Variant : CV161338 (GRCh38/hg38 16p13.2(chr16:8767999-8939742)x3) Homo sapiens

Symbol: CV161338
Name: GRCh38/hg38 16p13.2(chr16:8767999-8939742)x3
Condition: See cases [RCV000140292]
Clinical Significance: likely benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: ABAT   CARHSP1   LITAFD   PMM2   TMEM186   USP7  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000016.10:g.(?_8767999)_(8939742_?)dup
NC_000016.9:g.(?_8861856)_(9033599_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38168,767,999 - 8,939,742CLINVAR
GRCh37168,861,856 - 9,033,599CLINVAR
Build 36168,769,357 - 8,941,100CLINVAR
Cytogenetic Map1616p13.2CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487822
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-11-12
Status: ACTIVE



NHLBI Logo

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