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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099192copy number variation1nstd231human GRCh38.p12 chr1: 31,395,299-32,087,194 , GRCh37 chr1: 31,868,146-32,552,795 ADGRB2, COL16A1, 19 more genes
    nsv7052046inversion1nstd229human GRCh38 chr1: 31,418,659-31,418,765 , GRCh37.p13 chr1|NW_003571030.1: 18,748-18,854 , GRCh37.p13 chr1: 31,891,506-31,891,612 SERINC2
    nsv7044103inversion1nstd229human GRCh38 chr1: 26,905,652-33,050,814 , GRCh37.p13 chr1: 27,232,143-33,516,415 ADGRB2, SNORA16A, 169 more genes
    nsv6648709copy number variation1nstd229human GRCh38 chr1: 31,211,928-31,733,962 , GRCh37.p13 chr1: 31,684,775-32,199,563 PEF1, EEF1A1P46, 18 more genes
    nsv6648661copy number variation1nstd229human GRCh38 chr1: 31,235,267-31,736,466 , GRCh37.p13 chr1: 31,708,114-32,202,067 ZCCHC17, NKAIN1, 18 more genes
    nsv6648216copy number variation1nstd229human GRCh38 chr1: 31,374,301-31,420,100 , GRCh37.p13 chr1: 31,847,148-31,872,758 SERINC2, LOC105378623
    nsv6626374copy number variation1nstd224human GRCh37 chr1: 31,854,882-31,885,859 , GRCh38.p12 chr1: 31,382,035-31,413,012 LOC105378623, SERINC2
    nsv6329667copy number variation1nstd223human GRCh38 chr1: 31,417,401-31,420,600 , GRCh37.p13 chr1|NW_003571030.1: 17,490-20,689 , GRCh37.p13 chr1: 31,890,248-31,893,447 SERINC2
    nsv6322669copy number variation1nstd223human GRCh38 chr1: 31,416,789-31,443,525 , GRCh37.p13 chr1|NW_003571030.1: 16,878-43,614 , GRCh37.p13 chr1: 31,889,636-31,916,372 SERINC2
    nsv6313753copy number variation1nstd102humanUncertain significance GRCh37 chr1: 27,543,877-32,819,121 , GRCh38.p12 chr1: 27,217,386-32,353,520 DCDC2B, SNRNP40, 130 more genes
    nsv6290625copy number variation1nstd102humanUncertain significance GRCh37 chr1: 31,766,058-31,921,862 , GRCh38.p12 chr1: 31,293,211-31,449,015 FABP3, ZCCHC17, 4 more genes
    nsv6218909insertion1nstd214human GRCh38 chr1: 31,431,777-31,431,777 , GRCh37.p13 chr1: 31,904,624-31,904,624 , GRCh37.p13 chr1|NW_003571030.1: 31,866-31,866 SERINC2
    nsv6209970insertion2nstd214human GRCh38 chr1: 31,431,776-31,431,776 , GRCh37.p13 chr1|NW_003571030.1: 31,865-31,865 , GRCh37.p13 chr1: 31,904,623-31,904,623 SERINC2
    nsv6167089copy number variation1nstd214human GRCh38 chr1: 31,432,023-31,432,155 , GRCh37.p13 chr1|NW_003571030.1: 32,112-32,244 , GRCh37.p13 chr1: 31,904,870-31,905,002 SERINC2
    nsv6167067copy number variation1nstd214human GRCh38 chr1: 31,432,039-31,432,164 , GRCh37.p13 chr1: 31,904,886-31,905,011 , GRCh37.p13 chr1|NW_003571030.1: 32,128-32,253 SERINC2
    nsv6165034copy number variation1nstd214human GRCh38 chr1: 31,432,029-31,432,118 , GRCh37.p13 chr1: 31,904,876-31,904,965 , GRCh37.p13 chr1|NW_003571030.1: 32,118-32,207 SERINC2
    nsv6164266copy number variation1nstd214human GRCh38 chr1: 31,432,044-31,432,109 , GRCh37.p13 chr1|NW_003571030.1: 32,133-32,198 , GRCh37.p13 chr1: 31,904,891-31,904,956 SERINC2
    nsv6163330copy number variation1nstd214human GRCh38 chr1: 31,431,903-31,431,956 , GRCh37.p13 chr1|NW_003571030.1: 31,992-32,045 , GRCh37.p13 chr1: 31,904,750-31,904,803 SERINC2
    nsv6163203copy number variation1nstd214human GRCh38 chr1: 31,432,149-31,432,209 , GRCh37.p13 chr1|NW_003571030.1: 32,238-32,298 , GRCh37.p13 chr1: 31,904,996-31,905,056 SERINC2
    nsv6163020copy number variation1nstd214human GRCh38 chr1: 31,432,030-31,432,173 , GRCh37.p13 chr1|NW_003571030.1: 32,119-32,262 , GRCh37.p13 chr1: 31,904,877-31,905,020 SERINC2
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