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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1074045copy number variation1nstd99human GRCh37 chr7: 191,999-193,600 , GRCh38.p12 chr7: 191,999-193,600 , GRCh38.p12 chr7|NT_187558.1: 151,403-153,004 , GRCh38.p12 chr7|NT_187653.1: 184,320-185,921 FAM20C

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