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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3611747copy number variation2estd214human GRCh37 chr7: 78,321-231,876 , GRCh38.p12 chr7: 78,321-231,876 , GRCh38.p12 chr7|NT_187558.1: 34,420-157,952 , GRCh38.p12 chr7|NT_187653.1: 70,642-190,869 FAM20C, LINC03014, 5 more genes

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