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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967089insertion1nstd209human GRCh38 chr3: 111,993,483-111,993,483 , GRCh37.p13 chr3: 111,712,330-111,712,330 ABHD10
    nsv5675344mobile element insertion2nstd211human GRCh38 chr3: 111,993,495-111,993,495 , GRCh37.p13 chr3: 111,712,342-111,712,342 ABHD10
    nsv5623880insertion1nstd207human GRCh38 chr3: 111,993,483-111,993,483 , GRCh37.p13 chr3: 111,712,330-111,712,330 ABHD10
    nsv5555923sequence alteration1nstd206human GRCh38 chr3: 111,599,044-112,091,945 , GRCh37.p13 chr3: 111,317,891-111,810,792 ABHD10, PLCXD2, 10 more genes
    nsv5447691copy number variation1nstd206human GRCh38 chr3: 111,976,542-111,978,298 , GRCh37.p13 chr3: 111,695,389-111,697,145 ABHD10, PHLDB2
    nsv5396841mobile element insertion1nstd206human GRCh38 chr3: 111,993,495-111,993,546 , GRCh37.p13 chr3: 111,712,342-111,712,393 ABHD10
    nsv5302598copy number variation1nstd204human GRCh38.p13 chr3: 109,643,426-112,176,826 , GRCh37.p13 chr3: 109,362,273-111,895,673 , NECTIN3-AS1, 28 more genes
    nsv5229675copy number variation1nstd204human GRCh38.p13 chr3: 111,834,401-112,176,600 , GRCh37.p13 chr3: 111,553,248-111,895,447 TMPRSS7, PLCXD2, 10 more genes
    nsv5098676mobile element insertion1nstd203human GRCh38 chr3: 111,993,482-111,993,482 , GRCh37.p13 chr3: 111,712,329-111,712,329 ABHD10
    nsv5097592mobile element insertion1nstd203human GRCh38 chr3: 111,993,488-111,993,495 , GRCh37.p13 chr3: 111,712,335-111,712,342 ABHD10
    nsv5096372mobile element insertion1nstd203human GRCh38 chr3: 111,993,489-111,993,495 , GRCh37.p13 chr3: 111,712,336-111,712,342 ABHD10
    nsv5092118mobile element insertion1nstd203human GRCh38 chr3: 111,993,483-111,993,495 , GRCh37.p13 chr3: 111,712,330-111,712,342 ABHD10
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv4919552copy number variation1nstd200human GRCh38 chr3: 111,989,807-111,990,654 , GRCh37.p13 chr3: 111,708,654-111,709,501 ABHD10
    nsv4919551copy number variation1nstd200human GRCh38 chr3: 111,979,638-111,979,878 , GRCh37.p13 chr3: 111,698,485-111,698,725 ABHD10
    nsv4914627copy number variation1nstd200human GRCh38 chr3: 109,643,716-112,176,659 , GRCh37.p13 chr3: 109,362,563-111,895,506 , NECTIN3, 28 more genes
    nsv4914623copy number variation1nstd200human GRCh38 chr3: 109,310,668-113,023,370 , GRCh37.p13 chr3: 109,029,515-112,742,217 , CD200R1, 55 more genes
    nsv4794283copy number variation1nstd200human GRCh37 chr3: 109,362,563-111,895,506 , GRCh38.p12 chr3: 109,643,716-112,176,659 , LOC107984087, 28 more genes
    nsv4752860insertion1nstd199human GRCh37 chr3: 111,712,335-111,712,335 , GRCh38.p12 chr3: 111,993,488-111,993,488 ABHD10
    nsv4725501insertion1nstd186human GRCh37 chr3: 111,712,330-111,712,330 , GRCh38.p12 chr3: 111,993,483-111,993,483 ABHD10
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