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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3891006copy number variation2estd224human NCBI36 chr7: 136,005-318,150 , GRCh37.p13 chr7: 40,922-223,067 , GRCh38.p12 chr7: 43,902-223,067 , GRCh38.p12 chr7|NT_187558.1: 1-157,952 , GRCh38.p12 chr7|NT_187653.1: 36,223-190,869 FAM20C, LINC03014, 6 more genes

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