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Variant : CV154982 (GRCh38/hg38 Xq28(chrX:154154679-154332155)x3) Homo sapiens

Symbol: CV154982
Name: GRCh38/hg38 Xq28(chrX:154154679-154332155)x3
Condition: See cases [RCV000134633]
Clinical Significance: benign
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: OPN1LW   OPN1MW   OPN1MW2   OPN1MW3   TEX28   TKTL1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_154154679)_(154332155_?)dup
NC_000023.10:g.(?_153420154)_(153560505_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X154,154,679 - 154,332,155CLINVAR
GRCh37X153,420,154 - 153,560,505CLINVAR
Build 36X153,073,348 - 153,213,699CLINVAR
Cytogenetic MapXXq28CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9482213
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-10-15
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.