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Variant : CV162627 (GRCh38/hg38 Xp21.2(chrX:30027017-30322887)x0) Homo sapiens

Symbol: CV162627
Name: GRCh38/hg38 Xp21.2(chrX:30027017-30322887)x0
Condition: See cases [RCV000141381]
Clinical Significance: pathogenic
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: MAGEB1   MAGEB2   MAGEB3   MAGEB4   NR0B1  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_30027017)_(30322887_?)del
NC_000023.10:g.(?_30045134)_(30341004_?)del
Position
Human AssemblyChrPosition (strand)Source
GRCh38X30,027,017 - 30,322,887CLINVAR
GRCh37X30,045,134 - 30,341,004CLINVAR
Build 36X29,955,055 - 30,250,925CLINVAR
Cytogenetic MapXXp21.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9488906
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.