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Variant : CV159830 (GRCh38/hg38 Xq21.1-21.31(chrX:85396423-87061496)x3) Homo sapiens

Symbol: CV159830
Name: GRCh38/hg38 Xq21.1-21.31(chrX:85396423-87061496)x3
Condition: See cases [RCV000138988]
Clinical Significance: likely benign
Last Evaluated: 09/21/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CHM   DACH2   MIR1321   MIR361  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_85396423)_(87061496_?)dup
NC_000023.10:g.(?_84651428)_(86316499_?)dup
NC_000023.9:g.(?_84538084)_(86203155_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X85,396,423 - 87,061,496CLINVAR
GRCh37X84,651,428 - 86,316,499CLINVAR
Build 36X84,538,084 - 86,203,155CLINVAR
Cytogenetic MapXXq21.1-21.31CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9486520
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-09-06
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.