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Variant : CV154900 (GRCh38/hg38 Xq28(chrX:149797172-149916655)x3) Homo sapiens

Symbol: CV154900
Name: GRCh38/hg38 Xq28(chrX:149797172-149916655)x3
Condition: See cases [RCV000134551]
Clinical Significance: benign
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: LINC00850   MAGEA8   MAGEA8-AS1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_149797172)_(149916655_?)dup
NC_000023.10:g.(?_148878834)_(149084873_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X149,797,172 - 149,916,655CLINVAR
GRCh37X148,878,834 - 149,084,873CLINVAR
Build 36X148,686,631 - 148,835,531CLINVAR
Cytogenetic MapXXq28CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482131
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-09-10
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.