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Variant : CV383226 (GRCh37/hg19 11p11.2(chr11:48086949-48593349)x3) Homo sapiens

Symbol: CV383226
Name: GRCh37/hg19 11p11.2(chr11:48086949-48593349)x3
Condition: See cases [RCV000448171]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: OR4A47   OR4B1   OR4C3   OR4S1   OR4X1   OR4X2   PTPRJ  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
HGVS Name(s): NC_000011.9:g.(?_48086949)_(48593349_?)dup
Position
Human AssemblyChrPosition (strand)Source
GRCh371148,086,949 - 48,593,349CLINVAR
Cytogenetic Map1111p11.2CLINVAR




Additional Information

 
CRRD Object Information
CRRD ID: 12852881
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2017-10-03
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.