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Variant : CV157278 (GRCh38/hg38 10q24.32(chr10:101599084-101676484)x3) Homo sapiens

Symbol: CV157278
Name: GRCh38/hg38 10q24.32(chr10:101599084-101676484)x3
Condition: See cases [RCV000136700]
Clinical Significance: uncertain significance
Last Evaluated: 12/22/2010
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: DPCD   FBXW4   MIR3158-1   MIR3158-2  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000010.11:g.(?_101599084)_(101676484_?)dup
NC_000010.10:g.(?_103358841)_(103436241_?)dup
NC_000010.9:g.(?_103348831)_(103426231_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3810101,599,084 - 101,676,484CLINVAR
GRCh3710103,358,841 - 103,436,241CLINVAR
Build 3610103,348,831 - 103,426,231CLINVAR
Cytogenetic Map1010q24.32CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9484261
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.