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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv464243copy number variation1nstd27human NCBI35 chr7: 234,196-295,765 , GRCh37.p13 chr7: 139,113-200,682 , GRCh38.p12 chr7: 139,113-200,682 , GRCh38.p12 chr7|NT_187558.1: 95,035-157,952 , GRCh38.p12 chr7|NT_187653.1: 131,434-190,869 LINC03014, FAM20C, 3 more genes

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