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Variant : CV155515 (GRCh38/hg38 Xq23(chrX:113585463-113959540)x0) Homo sapiens

Symbol: CV155515
Name: GRCh38/hg38 Xq23(chrX:113585463-113959540)x0
Condition: See cases [RCV000135090]
Clinical Significance: benign
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: XACT  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_113585463)_(113959540_?)del
NC_000023.10:g.(?_112828750)_(113202825_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38X113,585,463 - 113,959,540CLINVAR
GRCh37X112,828,750 - 113,202,825CLINVAR
Build 36X112,715,406 - 113,089,090CLINVAR
Cytogenetic MapXXq23CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482663
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-11-05
Status: ACTIVE



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