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Variant : CV156619 (GRCh38/hg38 10q24.32(chr10:101434986-101689541)x3) Homo sapiens

Symbol: CV156619
Name: GRCh38/hg38 10q24.32(chr10:101434986-101689541)x3
Condition: See cases [RCV000136104]
Clinical Significance: uncertain significance
Last Evaluated: 11/30/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: BTRC   DPCD   FBXW4   MIR3158-1   MIR3158-2   POLL  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_101434986)_(101689541_?)dup
NC_000010.10:g.(?_103194743)_(103449298_?)dup
NC_000010.9:g.(?_103184733)_(103439288_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3810101,434,986 - 101,689,541CLINVAR
GRCh3710103,194,743 - 103,449,298CLINVAR
Build 3610103,184,733 - 103,439,288CLINVAR
Cytogenetic Map1010q24.32CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9483666
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-02-11
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.