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Variant : CV161759 (GRCh38/hg38 8p23.3(chr8:298209-456082)x3) Homo sapiens

Symbol: CV161759
Name: GRCh38/hg38 8p23.3(chr8:298209-456082)x3
Condition: See cases [RCV000140682]
Clinical Significance: benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: FAM87A   FBXO25  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000008.11:g.(?_298209)_(456082_?)dup
NC_000008.10:g.(?_248209)_(406082_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh388298,209 - 456,082CLINVAR
GRCh378248,209 - 406,082CLINVAR
Build 368238,209 - 396,082CLINVAR
Cytogenetic Map88p23.3CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 9488212
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-09-22
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.