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

Variant : CV553789 (GRCh37/hg19 2q22.3(chr2:145039778-145664032)x3) Homo sapiens

Symbol: CV553789
Name: GRCh37/hg19 2q22.3(chr2:145039778-145664032)x3
Condition: not provided [RCV000682094]
Clinical Significance: uncertain significance
Last Evaluated: 11/08/2017
Review Status: no assertion criteria provided
Related Genes: GTDC1   ZEB2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh372145,039,778 - 145,664,032CLINVAR
Cytogenetic Map22q22.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13794953
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2019-12-03
Status: ACTIVE



NHLBI Logo

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