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Variant : CV159927 (GRCh38/hg38 Xp11.23(chrX:49316774-49611138)x2) Homo sapiens

Symbol: CV159927
Name: GRCh38/hg38 Xp11.23(chrX:49316774-49611138)x2
Condition: See cases [RCV000139066]
Clinical Significance: likely benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: GAGE1   GAGE10   GAGE12B   GAGE12C   GAGE12D   GAGE12E   GAGE12F   GAGE12G   GAGE12H   GAGE12I   GAGE12J   GAGE13   GAGE2A   GAGE2B   GAGE2C   GAGE2D   GAGE2E   GAGE8  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_49316774)_(49611138_?)dup
NC_000023.10:g.(?_49173253)_(49370289_?)dup
NC_000023.9:g.(?_49060197)_(49262688_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X49,316,774 - 49,611,138CLINVAR
GRCh37X49,173,253 - 49,370,289 (+)CLINVAR
Build 36X49,060,197 - 49,262,688CLINVAR
Cytogenetic MapXXp11.23CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9486598
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.