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Variant : CV164213 (GRCh38/hg38 Xq13.3-21.1(chrX:76344954-77070816)x3) Homo sapiens

Symbol: CV164213
Name: GRCh38/hg38 Xq13.3-21.1(chrX:76344954-77070816)x3
Condition: See cases [RCV000142526]
Clinical Significance: uncertain significance
Last Evaluated: 12/13/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: MAGEE1   MIR325   MIR325HG   MIR384  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_76344954)_(77070816_?)dup
NC_000023.10:g.(?_75586665)_(76291236_?)dup
NC_000023.9:g.(?_75481757)_(76207627_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X76,344,954 - 77,070,816CLINVAR
GRCh37X75,586,665 - 76,291,236 (+)CLINVAR
Build 36X75,481,757 - 76,207,627CLINVAR
Cytogenetic MapXXq13.3-21.1CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9490124
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.