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Variant : CV165359 (GRCh38/hg38 Xp22.2-22.13(chrX:16967798-17710902)x3) Homo sapiens

Symbol: CV165359
Name: GRCh38/hg38 Xp22.2-22.13(chrX:16967798-17710902)x3
Condition: See cases [RCV000143672]
Clinical Significance: likely benign|uncertain significance
Last Evaluated: 07/18/2014
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: MIR4768   NHS   NHS-AS1   REPS2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_16967798)_(17710902_?)dup
NC_000023.10:g.(?_16985921)_(17729022_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X16,967,798 - 17,710,902CLINVAR
GRCh37X16,985,921 - 17,729,022CLINVAR
Build 36X16,895,842 - 17,638,943CLINVAR
Cytogenetic MapXXp22.2-22.13CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9491270
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.