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Variant : CV591986 (GRCh37/hg19 10q24.31-24.32(chr10:102841029-103558701)x3) Homo sapiens

Symbol: CV591986
Name: GRCh37/hg19 10q24.31-24.32(chr10:102841029-103558701)x3
Condition: not provided [RCV000737286]
Clinical Significance: benign
Last Evaluated: 01/26/2011
Review Status: no assertion criteria provided
Related Genes: BTRC   DPCD   FBXW4   FGF8   LBX1   NPM3   OGA   POLL   TLX1   TLX1NB  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh3710102,841,029 - 103,558,701CLINVAR
Cytogenetic Map1010q24.31-24.32CLINVAR




Additional Information

External Database Links
 
RGD Object Information
RGD ID: 14352529
Created: 2019-02-12
Species: Homo sapiens
Last Modified: 2020-02-04
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.