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    Number of Variants: 1

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv1149copy number variation1nstd2human NCBI35 chr13: 100,492,807-100,537,601 , GRCh37.p13 chr13: 101,694,806-101,739,600 , GRCh38.p12 chr13: 101,049,614-101,087,249 NALCN, NALCN-AS1

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