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Variant : CV162403 (GRCh38/hg38 10q23.31(chr10:89095288-89633544)x3) Homo sapiens

Symbol: CV162403
Name: GRCh38/hg38 10q23.31(chr10:89095288-89633544)x3
Condition: See cases [RCV000141185]
Clinical Significance: uncertain significance
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: CH25H   IFIT1   IFIT1B   IFIT2   IFIT3   IFIT5   LIPA   MIR107   PANK1   SLC16A12   SLC16A12-AS1  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_89095288)_(89633544_?)dup
NC_000010.10:g.(?_90855045)_(91393301_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381089,095,288 - 89,633,544CLINVAR
GRCh371090,855,045 - 91,393,301CLINVAR
Build 361090,845,025 - 91,383,281CLINVAR
Cytogenetic Map1010q23.31CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9488712
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-20
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.