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Items: 1 to 20 of 193

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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
    nsv6697363copy number variation1nstd229human GRCh38 chr2: 86,821,944-86,822,222 , GRCh37.p13 chr2: 87,049,067-87,049,345 CD8B, LOC105374846
    nsv6692786copy number variation1nstd229human GRCh38 chr2: 86,816,983-86,817,002 , GRCh37.p13 chr2: 87,044,106-87,044,125 LOC105374846, CD8B
    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
    nsv6686908copy number variation1nstd229human GRCh38 chr2: 86,822,845-86,832,952 , GRCh37.p13 chr2: 87,049,968-87,060,075 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
    nsv6680747copy number variation1nstd229human GRCh38 chr2: 86,844,744-86,847,025 , GRCh37.p13 chr2: 87,071,867-87,074,148 CD8B
    nsv6678960copy number variation1nstd229human GRCh38 chr2: 86,841,692-86,841,721 , GRCh37.p13 chr2: 87,068,815-87,068,844 CD8B
    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
    nsv6628226copy number variation1nstd224human GRCh37 chr2: 87,042,751-87,052,934 , GRCh38.p12 chr2: 86,815,628-86,825,811 LOC105374846, CD8B
    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
    nsv6550923inversion1nstd223human GRCh38 chr2: 86,832,449-86,833,185 , GRCh37.p13 chr2: 87,059,572-87,060,308 CD8B
    nsv6346248copy number variation1nstd223human GRCh38 chr2: 86,822,845-86,832,950 , GRCh37.p13 chr2: 87,049,968-87,060,073 CD8B
    nsv6343023copy number variation1nstd223human GRCh38 chr2: 86,860,901-86,865,600 , GRCh37.p13 chr2: 87,088,024-87,092,723 ANAPC1P1, CD8B
    nsv6341444copy number variation1nstd223human GRCh38 chr2: 86,847,643-86,849,781 , GRCh37.p13 chr2: 87,074,766-87,076,904 CD8B
    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
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