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Variant : CV384014 (GRCh37/hg19 11p11.2-11.12(chr11:47711244-48976284)x3) Homo sapiens

Symbol: CV384014
Name: GRCh37/hg19 11p11.2-11.12(chr11:47711244-48976284)x3
Condition: See cases [RCV000449235]
Clinical Significance: uncertain significance
Last Evaluated:
Review Status: no assertion criteria provided
Related Genes: AGBL2   FNBP4   NUP160   OR4A47   OR4B1   OR4C3   OR4S1   OR4X1   OR4X2   PTPRJ  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371147,711,244 - 48,976,284CLINVAR
Cytogenetic Map1111p11.2-11.12CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 12853931
Created: 2017-04-11
Species: Homo sapiens
Last Modified: 2020-02-04
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.