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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148181copy number variation1nstd102humanPathogenic GRCh38 chr7: 98,454,022-100,723,798 , GRCh37.p13 chr7: 98,083,334-100,321,421 LAMTOR4, PTCD1, 107 more genes
    nsv7098147copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,507,659-100,860,555 , GRCh38.p12 chr7: 98,910,036-101,217,274 SLC12A9, LOC105375423, 127 more genes
    nsv7053981inversion1nstd229human GRCh38 chr7: 99,772,347-99,788,507 , GRCh37.p13 chr7: 99,369,970-99,386,130 CYP3A4
    nsv7053608inversion1nstd229human GRCh38 chr7: 99,766,300-99,776,365 , GRCh37.p13 chr7: 99,363,923-99,373,988 CYP3A4
    nsv7052776inversion1nstd229human GRCh38 chr7: 96,709,838-100,726,550 , GRCh37.p13 chr7: 96,339,150-100,324,173 TMEM225B, PILRB, 141 more genes
    nsv6835743copy number variation1nstd229human GRCh38 chr7: 99,772,701-99,778,200 , GRCh37.p13 chr7: 99,370,324-99,375,823 CYP3A4
    nsv6821831copy number variation1nstd229human GRCh38 chr7: 99,731,352-99,768,692 , GRCh37.p13 chr7: 99,328,975-99,366,315 CYP3A7-CYP3A51P, ZSCAN25, 3 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6618643copy number variation1nstd223human GRCh38 chr7: 99,772,001-99,773,100 , GRCh37.p13 chr7: 99,369,624-99,370,723 CYP3A4
    nsv6608309copy number variation1nstd223human GRCh38 chr7: 99,690,031-99,813,799 , GRCh37.p13 chr7: 99,287,654-99,411,422 CYP3A4, CYP3A7-CYP3A51P, 4 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6312372copy number variation1nstd102humanPathogenic GRCh37 chr7: 98,983,338-100,860,555 , GRCh38.p12 chr7: 99,385,715-101,217,274 AZGP1P1, MOGAT3, 119 more genes
    nsv6290864copy number variation1nstd102humanUncertain significance GRCh37 chr7: 98,755,291-99,886,571 , GRCh38.p12 chr7: 99,157,668-100,288,948 LAMTOR4, OR2AE1, 62 more genes
    nsv6101547inversion1nstd212human GRCh38 chr7: 98,453,223-101,264,028 , GRCh37.p13 chr7: 98,082,535-100,907,309 , ACHE, 141 more genes
    nsv6079943insertion1nstd212human GRCh38 chr7: 99,771,312-99,771,312 , GRCh37.p13 chr7: 99,368,935-99,368,935 CYP3A4
    nsv6063836insertion1nstd212human GRCh38 chr7: 99,771,163-99,771,163 , GRCh37.p13 chr7: 99,368,786-99,368,786 CYP3A4
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 more genes
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5321926inversion1nstd204human GRCh37.p13 chr7: 93,899,155-99,360,080 , GRCh38.p13 chr7: 94,269,843-99,762,457 , CYP3A51P, 118 more genes
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