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

Variant : CV154582 (GRCh38/hg38 2q13(chr2:109959903-110360538)x3) Homo sapiens

Symbol: CV154582
Name: GRCh38/hg38 2q13(chr2:109959903-110360538)x3
Condition: See cases [RCV000134235]
Clinical Significance: benign
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINC01123   MALL   MIR4267   MIR4436B1   MIR4436B2   MTLN   NPHP1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000002.12:g.(?_109959903)_(110360538_?)dup
NC_000002.11:g.(?_110717480)_(111118115_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh382109,959,903 - 110,360,538CLINVAR
GRCh372110,717,480 - 111,118,115CLINVAR
Build 362110,074,769 - 110,552,653CLINVAR
Cytogenetic Map22q13CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9481815
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
Status: ACTIVE



NHLBI Logo

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