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Variant : CV160657 (GRCh38/hg38 Xp11.23(chrX:49293350-49343053)x2) Homo sapiens

Symbol: CV160657
Name: GRCh38/hg38 Xp11.23(chrX:49293350-49343053)x2
Condition: See cases [RCV000139702]
Clinical Significance: likely benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: GAGE10   GAGE12B   GAGE12I   GAGE12J   GAGE13   GAGE2B   GAGE2C   GAGE8   PPP1R3F  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_49293350)_(49343053_?)dup
NC_000023.10:g.(?_49149818)_(49218198_?)dup
NC_000023.9:g.(?_49036762)_(49105142_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X49,293,350 - 49,343,053 (+)CLINVAR
GRCh37X49,149,818 - 49,218,198CLINVAR
Build 36X49,036,762 - 49,105,142CLINVAR
Cytogenetic MapXXp11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487232
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-24
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.