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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1855insertion1nstd2human NCBI35 chr1: 92,222,832-92,253,354 , GRCh37.p13 chr1: 92,510,811-92,541,333 , GRCh38.p12 chr1: 92,045,254-92,075,776 EPHX4, SETSIP, 1 more genes

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