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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv471171copy number variation6nstd30human NCBI36 chr7: 140,736-295,765 , GRCh37.p13 chr7: 45,653-200,682 , GRCh38.p12 chr7: 45,653-200,682 , GRCh38.p12 chr7|NT_187558.1: 1,752-157,952 , GRCh38.p12 chr7|NT_187653.1: 37,974-190,869 FAM20C, LINC03014, 6 more genes

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