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

Variant : CV157550 (GRCh38/hg38 Xp21.1-11.4(chrX:37723259-38263335)x2) Homo sapiens

Symbol: CV157550
Name: GRCh38/hg38 Xp21.1-11.4(chrX:37723259-38263335)x2
Condition: See cases [RCV000136935]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CYBB   DYNLT3   H2AP   MIR548AJ2   SRPX   SYTL5   XK  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_37723259)_(38263335_?)dup
NC_000023.10:g.(?_37669767)_(38122588_?)dup
NC_000023.9:g.(?_37467451)_(38007532_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X37,723,259 - 38,263,335CLINVAR
GRCh37X37,669,767 - 38,122,588 (+)CLINVAR
Build 36X37,467,451 - 38,007,532CLINVAR
Cytogenetic MapXXp21.1-11.4CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9484496
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.