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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv520773copy number variation3nstd21human NCBI35 chr1: 156,736,032-156,748,642 , GRCh37.p13 chr1: 159,922,959-159,935,569 , GRCh38.p12 chr1: 159,953,169-159,965,779 SLAMF9, LINC01133

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