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Variant : CV161098 (GRCh38/hg38 11p15.5(chr11:200222-237805)x3) Homo sapiens

Symbol: CV161098
Name: GRCh38/hg38 11p15.5(chr11:200222-237805)x3
Condition: See cases [RCV000140063]
Clinical Significance: benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: BET1L   MIR6743   ODF3   PSMD13   RIC8A   SIRT3  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_200222)_(237805_?)dup
NC_000011.9:g.(?_200222)_(237805_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh3811200,222 - 237,805CLINVAR
GRCh3711200,222 - 237,805CLINVAR
Build 3611190,222 - 227,805CLINVAR
Cytogenetic Map1111p15.5CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487593
Created: 2014-09-09
Species: Homo sapiens
Last Modified: 2020-03-31
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.