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Variant : CV161256 (GRCh38/hg38 Xq22.3(chrX:104917368-104945823)x3) Homo sapiens

Symbol: CV161256
Name: GRCh38/hg38 Xq22.3(chrX:104917368-104945823)x3
Condition: See cases [RCV000140216]
Clinical Significance: likely benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: IL1RAPL2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_104917368)_(104945823_?)dup
NC_000023.10:g.(?_104162049)_(104190504_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X104,917,368 - 104,945,823CLINVAR
GRCh37X104,162,049 - 104,190,504CLINVAR
Build 36X104,048,705 - 104,077,160CLINVAR
Cytogenetic MapXXq22.3CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487746
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-09-17
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.