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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965210insertion1nstd209human GRCh38 chr3: 52,696,930-52,696,930 , GRCh37.p13 chr3: 52,730,946-52,730,946 GLT8D1
    nsv5678216mobile element insertion1nstd211human GRCh38 chr3: 52,703,817-52,703,817 , GRCh37.p13 chr3: 52,737,833-52,737,833 GLT8D1
    nsv5622152insertion1nstd207human GRCh38 chr3: 52,696,930-52,696,930 , GRCh37.p13 chr3: 52,730,946-52,730,946 GLT8D1
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5551821insertion1nstd206human GRCh38 chr3: 52,696,932-52,696,981 , GRCh37.p13 chr3: 52,730,948-52,730,997 GLT8D1
    nsv5442332copy number variation1nstd206human GRCh38 chr3: 52,690,553-52,692,565 , GRCh37.p13 chr3: 52,724,569-52,726,581 GNL3, SNORD69, 3 more genes
    nsv5413356mobile element insertion1nstd206human GRCh38 chr3: 52,703,817-52,703,868 , GRCh37.p13 chr3: 52,737,833-52,737,884 GLT8D1
    nsv5066405mobile element insertion1nstd203human GRCh38 chr3: 52,703,802-52,703,817 , GRCh37.p13 chr3: 52,737,818-52,737,833 GLT8D1
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4911347copy number variation1nstd200human GRCh38 chr3: 51,769,352-52,724,007 , GRCh37.p13 chr3: 51,803,368-52,758,023 , ACY1, 55 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4790701copy number variation1nstd200human GRCh37 chr3: 51,803,368-52,758,023 , GRCh38.p12 chr3: 51,769,352-52,724,007 , SNORD19B, 55 more genes
    nsv4759850insertion1nstd199human GRCh37 chr3: 52,730,941-52,730,941 , GRCh38.p12 chr3: 52,696,925-52,696,925 GLT8D1
    nsv4726011insertion1nstd186human GRCh37 chr3: 52,730,946-52,730,946 , GRCh38.p12 chr3: 52,696,930-52,696,930 GLT8D1
    nsv4679783copy number variation1nstd189human GRCh37.p13 chr3: 52,082,781-53,128,685 , GRCh38.p12 chr3: 52,048,765-53,094,669 , ALAS1, 50 more genes
    nsv4673975copy number variation1nstd102humanUncertain significance GRCh37 chr3: 51,247,306-53,069,942 , GRCh38.p12 chr3: 51,209,875-53,035,926 RRP9, LOC100301990, 76 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4556342insertion1nstd166human GRCh37.p13 chr3: 52,730,946-52,730,946 , GRCh38.p12 chr3: 52,696,930-52,696,930 GLT8D1
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