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Items: 1 to 20 of 173

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7045520inversion1nstd229human GRCh38 chr2: 86,706,307-86,887,942 , GRCh37.p13 chr2: 86,933,430-87,115,065 CD8B, ANAPC1P1, 4 more genes
    nsv7039831inversion1nstd229human GRCh38 chr2: 86,881,149-86,881,219 , GRCh37.p13 chr2: 87,108,272-87,108,342 ANAPC1P1
    nsv6692564copy number variation1nstd229human GRCh38 chr2: 86,861,699-86,861,737 , GRCh37.p13 chr2: 87,088,822-87,088,860 CD8B, ANAPC1P1
    nsv6691145copy number variation1nstd229human GRCh38 chr2: 86,861,059-86,865,568 , GRCh37.p13 chr2: 87,088,182-87,092,691 ANAPC1P1, CD8B
    nsv6685229copy number variation1nstd229human GRCh38 chr2: 86,813,401-86,893,600 , GRCh37.p13 chr2: 87,040,524-87,120,723 CD8B, ANAPC1P1, 1 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6628358copy number variation1nstd224human GRCh37 chr2: 86,969,771-87,171,150 , GRCh38.p12 chr2: 86,742,648-86,944,027 CD8A, CD8B, 6 more genes
    nsv6628159copy number variation1nstd224human GRCh37 chr2: 86,974,049-87,123,114 , GRCh38.p12 chr2: 86,746,926-86,895,991 CD8B, RMND5A, 3 more genes
    nsv6350117copy number variation1nstd223human GRCh38 chr2: 86,872,301-86,875,500 , GRCh37.p13 chr2: 87,099,424-87,102,623 ANAPC1P1
    nsv6343023copy number variation1nstd223human GRCh38 chr2: 86,860,901-86,865,600 , GRCh37.p13 chr2: 87,088,024-87,092,723 ANAPC1P1, CD8B
    nsv6336597copy number variation1nstd223human GRCh38 chr2: 86,883,401-86,884,300 , GRCh37.p13 chr2: 87,110,524-87,111,423 ANAPC1P1
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6313890copy number variation1nstd102humanPathogenic GRCh37 chr2: 82,486,900-87,322,042 , GRCh38.p12 chr2: 82,259,776-87,094,919 LOC105374836, LOC105374833, 93 more genes
    nsv5873278copy number variation1nstd209human GRCh38 chr2: 86,884,248-86,884,811 , GRCh37.p13 chr2: 87,111,371-87,111,934 ANAPC1P1
    nsv5616772insertion1nstd207human GRCh38 chr2: 86,863,038-86,863,038 , GRCh37.p13 chr2: 87,090,161-87,090,161 ANAPC1P1
    nsv5616657insertion1nstd207human GRCh38 chr2: 86,863,034-86,863,034 , GRCh37.p13 chr2: 87,090,157-87,090,157 ANAPC1P1
    nsv5609909insertion1nstd207human GRCh38 chr2: 86,882,718-86,882,718 , GRCh37.p13 chr2: 87,109,841-87,109,841 ANAPC1P1
    nsv5563141inversion1nstd206human GRCh38 chr2: 86,868,837-86,883,576 , GRCh37.p13 chr2: 87,095,960-87,110,699 ANAPC1P1
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
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