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

Variant : CV675289 (GRCh37/hg19 3p26.1(chr3:4276014-4643555)x1) Homo sapiens

Symbol: CV675289
Name: GRCh37/hg19 3p26.1(chr3:4276014-4643555)x1
Condition: not provided [RCV000848388]
Clinical Significance: pathogenic
Last Evaluated: 12/06/2017
Review Status: no assertion criteria provided
Related Genes: ITPR1   SETMAR   SUMF1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3734,276,014 - 4,643,555CLINVAR
Cytogenetic Map33p26.1CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14979945
Created: 2019-10-08
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.