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Variant : CV161117 (GRCh38/hg38 Xq23(chrX:110359806-111260954)x3) Homo sapiens

Symbol: CV161117
Name: GRCh38/hg38 Xq23(chrX:110359806-111260954)x3
Condition: See cases [RCV000140082]
Clinical Significance: uncertain significance
Last Evaluated: 04/09/2013
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: AMMECR1   CAPN6   CHRDL1   PAK3   RTL9  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_110359806)_(111260954_?)dup
NC_000023.10:g.(?_109603034)_(110504182_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X110,359,806 - 111,260,954CLINVAR
GRCh37X109,603,034 - 110,504,182CLINVAR
Build 36X109,489,690 - 110,390,838CLINVAR
Cytogenetic MapXXq23CLINVAR



References - uncurated

Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9487612
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-17
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.