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Variant : CV162698 (GRCh38/hg38 Xp22.2-22.13(chrX:17310142-17506167)x3) Homo sapiens

Symbol: CV162698
Name: GRCh38/hg38 Xp22.2-22.13(chrX:17310142-17506167)x3
Condition: See cases [RCV000141446]
Clinical Significance: uncertain significance
Last Evaluated: 10/15/2012
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: MIR4768   NHS  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_17310142)_(17506167_?)dup
NC_000023.10:g.(?_17328265)_(17524290_?)dup
NC_000023.9:g.(?_17238186)_(17434211_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X17,310,142 - 17,506,167CLINVAR
GRCh37X17,328,265 - 17,524,290CLINVAR
Build 36X17,238,186 - 17,434,211CLINVAR
Cytogenetic MapXXp22.2-22.13CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9488971
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.