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Variant : CV161449 (GRCh38/hg38 Xq26.2(chrX:131784025-131835887)x3) Homo sapiens

Symbol: CV161449
Name: GRCh38/hg38 Xq26.2(chrX:131784025-131835887)x3
Condition: See cases [RCV000140402]
Clinical Significance: benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: FIRRE  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000023.11:g.(?_131784025)_(131835887_?)dup
NC_000023.10:g.(?_130918053)_(130969915_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh38X131,784,025 - 131,835,887CLINVAR
GRCh37X130,918,053 - 130,969,915CLINVAR
Build 36X130,745,734 - 130,797,596CLINVAR
Cytogenetic MapXXq26.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487932
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2019-11-12
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.