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Variant : CV592206 (GRCh37/hg19 11p11.2(chr11:48203984-48391207)x0) Homo sapiens

Symbol: CV592206
Name: GRCh37/hg19 11p11.2(chr11:48203984-48391207)x0
Condition: not provided [RCV000737506]
Clinical Significance: benign
Last Evaluated: 12/06/2011
Review Status: no assertion criteria provided
Related Genes: OR4B1   OR4C3   OR4S1   OR4X1   OR4X2  
Variant Type: copy number loss (SO:0001743)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371148,203,984 - 48,391,207CLINVAR
Cytogenetic Map1111p11.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 14352869
Created: 2019-02-12
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.