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

Variant : CV158301 (GRCh38/hg38 Xp22.12(chrX:20007955-20579523)x2) Homo sapiens

Symbol: CV158301
Name: GRCh38/hg38 Xp22.12(chrX:20007955-20579523)x2
Condition: See cases [RCV000137623]
Clinical Significance: uncertain significance
Last Evaluated: 04/05/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: EIF1AX   EIF1AX-AS1   MAP7D2   MIR23C   RPS6KA3   SCARNA9L  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_20007955)_(20579523_?)dup
NC_000023.10:g.(?_20026073)_(20597641_?)dup
NC_000023.9:g.(?_19935994)_(20507562_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X20,007,955 - 20,579,523CLINVAR
GRCh37X20,026,073 - 20,597,641CLINVAR
Build 36X19,935,994 - 20,507,562CLINVAR
Cytogenetic MapXXp22.12CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9485176
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.