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

Variant : CV555045 (GRCh37/hg19 11p11.2-11.12(chr11:48065950-48893177)x3) Homo sapiens

Symbol: CV555045
Name: GRCh37/hg19 11p11.2-11.12(chr11:48065950-48893177)x3
Condition: not provided [RCV000683350]
Clinical Significance: likely benign
Last Evaluated: 10/27/2017
Review Status: no assertion criteria provided
Related Genes: OR4A47   OR4B1   OR4C3   OR4S1   OR4X1   OR4X2   PTPRJ  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371148,065,950 - 48,893,177CLINVAR
Cytogenetic Map1111p11.2-11.12CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13796489
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-02-11
Status: ACTIVE



NHLBI Logo

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