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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5721805mobile element insertion2nstd211human GRCh38 chr6: 52,521,698-52,521,698 , GRCh37.p13 chr6: 52,386,496-52,386,496 TRAM2
    nsv5690254mobile element insertion1nstd211human GRCh38 chr6: 52,567,718-52,567,718 , GRCh37.p13 chr6: 52,432,516-52,432,516 TRAM2
    nsv5686302mobile element insertion1nstd211human GRCh38 chr6: 52,518,048-52,518,048 , GRCh37.p13 chr6: 52,382,846-52,382,846 TRAM2
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5541620insertion1nstd206human GRCh38 chr6: 52,577,090-52,577,141 , GRCh37.p13 chr6: 52,441,888-52,441,939 TRAM2, TRAM2-AS1
    nsv5537787insertion1nstd206human GRCh38 chr6: 52,521,714-52,521,749 , GRCh37.p13 chr6: 52,386,512-52,386,547 TRAM2
    nsv5466434copy number variation1nstd206human GRCh38 chr6: 52,526,849-52,528,584 , GRCh37.p13 chr6: 52,391,647-52,393,382 TRAM2
    nsv5461874copy number variation1nstd206human GRCh38 chr6: 52,505,903-52,505,965 , GRCh37.p13 chr6: 52,370,701-52,370,763 TRAM2
    nsv5412937mobile element insertion1nstd206human GRCh38 chr6: 52,518,048-52,518,099 , GRCh37.p13 chr6: 52,382,846-52,382,897 TRAM2
    nsv5397093mobile element insertion1nstd206human GRCh38 chr6: 52,567,718-52,567,769 , GRCh37.p13 chr6: 52,432,516-52,432,567 TRAM2
    nsv5381452copy number variation1nstd102humanUncertain significance GRCh37 chr6: 51,930,764-52,906,034 , GRCh38.p12 chr6: 52,065,966-53,041,236 GSTA4, LOC730101, 30 more genes
    nsv5362980translocation1nstd200human GRCh38 chr6: 52,505,965-52,505,965 , GRCh38 chr6: 52,505,903-52,505,903 , GRCh37.p13 chr6: 52,370,763-52,370,763 , GRCh37.p13 chr6: 52,370,701-52,370,701 TRAM2
    nsv5317862copy number variation1nstd204human GRCh38.p13 chr6: 52,520,532-52,521,113 , GRCh37.p13 chr6: 52,385,330-52,385,911 TRAM2
    nsv5116056mobile element insertion1nstd203human GRCh38 chr6: 52,567,705-52,567,718 , GRCh37.p13 chr6: 52,432,503-52,432,516 TRAM2
    nsv4941441copy number variation1nstd200human GRCh38 chr6: 52,554,219-52,554,269 , GRCh37.p13 chr6: 52,419,017-52,419,067 TRAM2
    nsv4941440copy number variation1nstd200human GRCh38 chr6: 52,526,849-52,528,584 , GRCh37.p13 chr6: 52,391,647-52,393,382 TRAM2
    nsv4941439copy number variation1nstd200human GRCh38 chr6: 52,524,738-52,524,825 , GRCh37.p13 chr6: 52,389,536-52,389,623 TRAM2
    nsv4941438copy number variation1nstd200human GRCh38 chr6: 52,501,889-52,502,033 , GRCh37.p13 chr6: 52,366,687-52,366,831 TRAM2
    nsv4816404copy number variation1nstd200human GRCh37 chr6: 52,385,358-52,385,889 , GRCh38.p12 chr6: 52,520,560-52,521,091 TRAM2
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
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