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Items: 2

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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv23045sequence alteration1estd20human NCBI36 chr3: 32,313,997-32,314,528 , GRCh37.p13 chr3: 32,338,993-32,339,524 , GRCh38.p12 chr3: 32,297,501-32,298,032 CMTM8
    esv21431copy number variation1estd20human NCBI36 chr3: 32,313,997-32,314,528 , GRCh37.p13 chr3: 32,338,993-32,339,524 , GRCh38.p12 chr3: 32,297,501-32,298,032 CMTM8

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