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

Variant : CV436177 (GRCh37/hg19 1p36.23-36.22(chr1:8855705-9389530)x1) Homo sapiens

Symbol: CV436177
Name: GRCh37/hg19 1p36.23-36.22(chr1:8855705-9389530)x1
Condition: See cases [RCV000510311]
Clinical Significance: likely benign
Last Evaluated: 06/22/2015
Review Status: no assertion criteria provided
Related Genes: CA6   ENO1   ENO1-AS1   GPR157   H6PD   MIR34A   RERE   SLC2A5   SLC2A7   SPSB1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3718,855,705 - 9,389,530CLINVAR
Cytogenetic Map11p36.23-36.22CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443290
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-03-31
Status: ACTIVE



NHLBI Logo

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