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Variant : CV161024 (GRCh38/hg38 11p11.2(chr11:48110126-48623909)x3) Homo sapiens

Symbol: CV161024
Name: GRCh38/hg38 11p11.2(chr11:48110126-48623909)x3
Condition: See cases [RCV000139996]
Clinical Significance: likely benign
Last Evaluated: 04/30/2011
Review Status: classified by single submitter|no assertion criteria provided
Related Genes: OR4A47   OR4B1   OR4C3   OR4C5   OR4S1   OR4X1   OR4X2   PTPRJ  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.10:g.(?_48110126)_(48623909_?)dup
NC_000011.9:g.(?_48131678)_(48645461_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh381148,110,126 - 48,623,909CLINVAR
GRCh371148,131,678 - 48,645,461CLINVAR
Build 361148,088,254 - 48,602,037CLINVAR
Cytogenetic Map1111p11.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 9487526
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.