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Variant : CV438501 (GRCh37/hg19 12q22(chr12:95094003-95254150)x3) Homo sapiens

Symbol: CV438501
Name: GRCh37/hg19 12q22(chr12:95094003-95254150)x3
Condition: not provided [RCV000513595]
Clinical Significance: likely benign
Last Evaluated: 06/23/2017
Review Status: criteria provided, single submitter|no assertion criteria provided
Related Genes: MIR492  
Variant Type: copy number gain (SO:0001742)
Evidence: clinical testing
Human AssemblyChrPosition (strand)Source
GRCh371295,094,003 - 95,254,150CLINVAR
Cytogenetic Map1212q22CLINVAR

Additional Information

External Database Links
CRRD Object Information
CRRD ID: 13446345
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.