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

Variant : CV154876 (GRCh38/hg38 Xp21.1(chrX:32557406-32754551)x0) Homo sapiens

Symbol: CV154876
Name: GRCh38/hg38 Xp21.1(chrX:32557406-32754551)x0
Condition: See cases [RCV000134527]
Clinical Significance: pathogenic
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: DMD   MIR3915   MIR548F5  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_32557406)_(32754551_?)del
NC_000023.10:g.(?_32575523)_(32772668_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38X32,557,406 - 32,754,551CLINVAR
GRCh37X32,575,523 - 32,772,668CLINVAR
Build 36X32,485,444 - 32,682,589CLINVAR
Cytogenetic MapXXp21.1CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9482107
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.