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Variant : CV435948 (GRCh37/hg19 11p11.2-11.12(chr11:47748831-48985791)x3) Homo sapiens

Symbol: CV435948
Name: GRCh37/hg19 11p11.2-11.12(chr11:47748831-48985791)x3
Condition: See cases [RCV000510265]
Clinical Significance: uncertain significance
Last Evaluated: 11/18/2014
Review Status: no assertion criteria provided
Related Genes: FNBP4   NUP160   OR4A47   OR4B1   OR4C3   OR4S1   OR4X1   OR4X2   PTPRJ  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh371147,748,831 - 48,985,791CLINVAR
Cytogenetic Map1111p11.2-11.12CLINVAR

References - uncurated

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 13443245
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-02-20
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.