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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5888879copy number variation1nstd209human GRCh38 chr3: 114,303,505-114,303,598 , GRCh37.p13 chr3: 114,022,352-114,022,445 TIGIT
    nsv5674224copy number variation1nstd102humanPathogenic GRCh37 chr3: 113,623,035-114,368,128 , GRCh38.p12 chr3: 113,904,188-114,649,281 VPS26AP1, ATOSBP1, 14 more genes
    nsv5610070insertion3nstd207human GRCh38 chr3: 114,303,630-114,303,630 , GRCh37.p13 chr3: 114,022,477-114,022,477 TIGIT
    nsv5565544copy number variation1nstd207human GRCh38 chr3: 114,303,505-114,303,598 , GRCh37.p13 chr3: 114,022,352-114,022,445 TIGIT
    nsv5556590sequence alteration1nstd206human GRCh38 chr3: 114,305,082-114,307,996 , GRCh37.p13 chr3: 114,023,929-114,026,843 TIGIT
    nsv5448480copy number variation1nstd206human GRCh38 chr3: 114,258,113-114,296,672 , GRCh37.p13 chr3: 113,976,960-114,015,519 TIGIT
    nsv5443684copy number variation1nstd206human GRCh38 chr3: 114,294,209-114,297,506 , GRCh37.p13 chr3: 114,013,056-114,016,353 TIGIT
    nsv5442649copy number variation1nstd206human GRCh38 chr3: 114,305,048-114,308,038 , GRCh37.p13 chr3: 114,023,895-114,026,885 TIGIT
    nsv5435438copy number variation1nstd206human GRCh38 chr3: 114,303,516-114,303,595 , GRCh37.p13 chr3: 114,022,363-114,022,442 TIGIT
    nsv5434181copy number variation1nstd206human GRCh38 chr3: 114,291,663-114,293,476 , GRCh37.p13 chr3: 114,010,510-114,012,323 TIGIT
    nsv5385555copy number variation1nstd186human GRCh37 chr3: 114,022,389-114,022,440 , GRCh38.p12 chr3: 114,303,542-114,303,593 TIGIT
    nsv5346430translocation1nstd200human GRCh38 chr3: 114,299,088-114,299,088 , GRCh38 chr3: 114,307,996-114,307,996 , GRCh37.p13 chr3: 114,026,843-114,026,843 , GRCh37.p13 chr3: 114,017,935-114,017,935 TIGIT
    nsv5300398copy number variation1nstd204human GRCh37.p13 chr3: 114,030,464-114,031,529 , GRCh38.p13 chr3: 114,311,617-114,312,682 ZBTB20, TIGIT
    nsv5094112mobile element insertion1nstd203human GRCh38 chr3: 114,308,646-114,308,656 , GRCh37.p13 chr3: 114,027,493-114,027,503 TIGIT
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5031637inversion1nstd200human GRCh38 chr3: 112,181,184-125,673,487 , GRCh37.p13 chr3: 111,900,031-125,392,331 , ARHGAP31, 218 more genes
    nsv4919618copy number variation1nstd200human GRCh38 chr3: 114,309,409-114,310,271 , GRCh37.p13 chr3: 114,028,256-114,029,118 TIGIT
    nsv4919617copy number variation1nstd200human GRCh38 chr3: 114,303,542-114,303,593 , GRCh37.p13 chr3: 114,022,389-114,022,440 TIGIT
    nsv4914663copy number variation1nstd200human GRCh38 chr3: 114,258,097-114,296,672 , GRCh37.p13 chr3: 113,976,944-114,015,519 TIGIT
    nsv4734636copy number variation1nstd199human GRCh37 chr3: 114,022,355-114,022,451 , GRCh38.p12 chr3: 114,303,508-114,303,604 TIGIT
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