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Variant : CV436011 (GRCh37/hg19 11p11.2-11.12(chr11:48116086-48913631)x3) Homo sapiens

Symbol: CV436011
Name: GRCh37/hg19 11p11.2-11.12(chr11:48116086-48913631)x3
Condition: See cases [RCV000510344]
Clinical Significance: likely benign
Last Evaluated: 06/23/2014
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
Position
Human AssemblyChrPosition (strand)Source
GRCh371148,116,086 - 48,913,631CLINVAR
Cytogenetic Map1111p11.2-11.12CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13443323
Created: 2017-11-07
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.