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Variant : CV157743 (GRCh38/hg38 Xq28(chrX:149570094-150079450)x3) Homo sapiens

Symbol: CV157743
Name: GRCh38/hg38 Xq28(chrX:149570094-150079450)x3
Condition: See cases [RCV000137090]
Clinical Significance: likely benign
Last Evaluated: 03/09/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CXorf40B   HSFX1   HSFX2   HSFX4   LINC00850   LINC00894   MAGEA11   MAGEA8   MAGEA8-AS1   MAGEA9   MAGEA9B   TMEM185A  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_149570094)_(150079450_?)dup
NW_004070890.2:g.(?_5094492)_(5603848_?)dup
NC_000023.9:g.(?_148459544)_(148998339_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X149,570,094 - 150,079,450CLINVAR
Build 36X148,459,544 - 148,998,339CLINVAR
Cytogenetic MapXXq28CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9484649
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.