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Items: 1 to 20 of 467

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051246inversion1nstd229human GRCh38 chr2: 99,001,430-99,852,801 , GRCh37.p13 chr2: 99,617,893-100,469,263 EIF5B, MITD1, 12 more genes
    nsv7048632inversion1nstd229human GRCh38 chr2: 99,012,932-99,012,943 , GRCh37.p13 chr2: 99,629,395-99,629,406 TSGA10
    nsv6697253copy number variation1nstd229human GRCh38 chr2: 99,129,103-99,140,841 , GRCh37.p13 chr2: 99,745,566-99,757,304 TSGA10, C2orf15
    nsv6696870copy number variation1nstd229human GRCh38 chr2: 99,097,779-99,143,142 , GRCh37.p13 chr2: 99,714,242-99,759,605 TSGA10, C2orf15, 1 more genes
    nsv6696832copy number variation1nstd229human GRCh38 chr2: 99,108,024-99,111,522 , GRCh37.p13 chr2: 99,724,487-99,727,985 TSGA10
    nsv6692523copy number variation1nstd229human GRCh38 chr2: 99,045,450-99,050,060 , GRCh37.p13 chr2: 99,661,913-99,666,523 TSGA10
    nsv6688077copy number variation1nstd229human GRCh38 chr2: 99,123,087-99,127,087 , GRCh37.p13 chr2: 99,739,550-99,743,550 TSGA10
    nsv6687006copy number variation1nstd229human GRCh38 chr2: 99,106,429-99,166,652 , GRCh37.p13 chr2: 99,722,892-99,783,115 C2orf15, MITD1, 2 more genes
    nsv6685425copy number variation1nstd229human GRCh38 chr2: 98,995,511-98,995,607 , GRCh37.p13 chr2: 99,611,974-99,612,070 TSGA10
    nsv6685319copy number variation1nstd229human GRCh38 chr2: 99,144,695-99,148,847 , GRCh37.p13 chr2: 99,761,158-99,765,310 TSGA10, C2orf15
    nsv6684767copy number variation1nstd229human GRCh38 chr2: 99,144,685-99,152,666 , GRCh37.p13 chr2: 99,761,148-99,769,129 C2orf15, TSGA10
    nsv6682518copy number variation1nstd229human GRCh38 chr2: 99,148,943-99,152,665 , GRCh37.p13 chr2: 99,765,406-99,769,128 TSGA10, C2orf15
    nsv6681404copy number variation1nstd229human GRCh38 chr2: 99,082,338-99,087,460 , GRCh37.p13 chr2: 99,698,801-99,703,923 TSGA10
    nsv6678416copy number variation1nstd229human GRCh38 chr2: 99,000,322-99,059,301 , GRCh37.p13 chr2: 99,616,785-99,675,764 TSGA10
    nsv6636315copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 95,341,388-100,340,514 , GRCh38.p12 chr2: 94,675,663-99,724,052 ADRA2B, ATP5F1BP1, 130 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
    nsv6555551inversion1nstd223human GRCh38 chr2: 99,146,004-99,146,935 , GRCh37.p13 chr2: 99,762,467-99,763,398 TSGA10, C2orf15
    nsv6547825inversion1nstd223human GRCh38 chr2: 99,135,836-99,136,991 , GRCh37.p13 chr2: 99,752,299-99,753,454 TSGA10
    nsv6540663inversion1nstd223human GRCh38 chr2: 99,077,855-99,078,195 , GRCh37.p13 chr2: 99,694,318-99,694,658 TSGA10
    nsv6539785inversion1nstd223human GRCh38 chr2: 99,022,343-99,023,250 , GRCh37.p13 chr2: 99,638,806-99,639,713 TSGA10
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