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Variant : CV437192 (GRCh37/hg19 11p11.2-11.12(chr11:48149532-49434855)x3) Homo sapiens

Symbol: CV437192
Name: GRCh37/hg19 11p11.2-11.12(chr11:48149532-49434855)x3
Condition: See cases [RCV000511753]
Clinical Significance: uncertain significance
Last Evaluated: 03/26/2015
Review Status: no assertion criteria provided
Related Genes: FOLH1   OR4A47   OR4B1   OR4C3   OR4S1   OR4X1   OR4X2   PTPRJ   TRIM49B   TRIM64C  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371148,149,532 - 49,434,855CLINVAR
Cytogenetic Map1111p11.2-11.12CLINVAR



References - uncurated

Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13444722
Created: 2017-11-07
Species: Homo sapiens
Last Modified: 2020-02-11
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.