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Variant : CV555098 (GRCh37/hg19 12p13.2(chr12:11043965-11260347)x4) Homo sapiens

Symbol: CV555098
Name: GRCh37/hg19 12p13.2(chr12:11043965-11260347)x4
Condition: not provided [RCV000683403]
Clinical Significance: likely benign
Last Evaluated: 09/22/2017
Review Status: no assertion criteria provided
Related Genes: PRH2   TAS2R13   TAS2R14   TAS2R19   TAS2R20   TAS2R31   TAS2R43   TAS2R46   TAS2R50  
Variant Type: copy number gain (SO:0001742)
Source: CLINVAR
Evidence: clinical testing
Position
Human AssemblyChrPosition (strand)Source
GRCh371211,043,965 - 11,260,347CLINVAR
Cytogenetic Map1212p13.2CLINVAR




Additional Information

External Database Links
 
CRRD Object Information
CRRD ID: 13796634
Created: 2018-10-09
Species: Homo sapiens
Last Modified: 2020-08-04
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.