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Variant : CV163833 (GRCh38/hg38 Xq21.2(chrX:85881568-86228805)x3) Homo sapiens

Symbol: CV163833
Name: GRCh38/hg38 Xq21.2(chrX:85881568-86228805)x3
Condition: See cases [RCV000142232]
Clinical Significance: uncertain significance
Last Evaluated: 03/10/2014
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CHM   DACH2   MIR361  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_85881568)_(86228805_?)dup
NC_000023.10:g.(?_85136573)_(85483808_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X85,881,568 - 86,228,805CLINVAR
GRCh37X85,136,573 - 85,483,808CLINVAR
Build 36X85,023,229 - 85,370,464CLINVAR
Cytogenetic MapXXq21.2CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9489751
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.