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    Number of Variants: 2

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4405926copy number variation1nstd174human GRCh37 chr3: 32,338,801-32,339,852 , GRCh38.p12 chr3: 32,297,309-32,298,360 CMTM8
    esv3595770copy number variation39estd214human GRCh37 chr3: 32,338,768-32,339,755 , GRCh38.p12 chr3: 32,297,276-32,298,263 CMTM8

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