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Items: 1 to 20 of 424

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130457insertion1nstd186human GRCh37 chr15: 80,718,429-80,718,451 , GRCh38.p12 chr15: 80,426,087-80,426,109 ARNT2
    nsv6113736mobile element insertion1nstd186human GRCh37 chr15: 80,858,574-80,858,625 , GRCh38.p12 chr15: 80,566,233-80,566,284 ARNT2
    nsv5977149insertion1nstd209human GRCh38 chr15: 80,522,843-80,522,843 , GRCh37.p13 chr15: 80,815,184-80,815,184 ARNT2
    nsv5973275insertion1nstd209human GRCh38 chr15: 80,426,058-80,426,058 , GRCh37.p13 chr15: 80,718,400-80,718,400 ARNT2
    nsv5943006copy number variation1nstd209human GRCh38 chr15: 80,409,339-80,409,583 , GRCh37.p13 chr15: 80,701,681-80,701,925 ARNT2
    nsv5941875copy number variation1nstd209human GRCh38 chr15: 80,504,468-80,507,591 , GRCh37.p13 chr15: 80,796,809-80,799,932 ARNT2
    nsv5935349copy number variation1nstd209human GRCh38 chr15: 77,970,674-82,312,707 , GRCh37.p13 chr15: 78,263,016-82,605,043 , ST20, 91 more genes
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5929988copy number variation1nstd209human GRCh38 chr15: 80,444,833-80,444,891 , GRCh37.p13 chr15: 80,737,174-80,737,232 ARNT2
    nsv5848065copy number variation1nstd209human GRCh38 chr15: 80,504,479-80,508,006 , GRCh37.p13 chr15: 80,796,820-80,800,347 ARNT2
    nsv5710854mobile element insertion1nstd211human GRCh38 chr15: 80,543,214-80,543,214 , GRCh37.p13 chr15: 80,835,555-80,835,555 ARNT2
    nsv5709486mobile element insertion2nstd211human GRCh38 chr15: 80,566,233-80,566,233 , GRCh37.p13 chr15: 80,858,574-80,858,574 ARNT2
    nsv5699110mobile element insertion2nstd211human GRCh38 chr15: 80,522,856-80,522,856 , GRCh37.p13 chr15: 80,815,197-80,815,197 ARNT2
    nsv5694942mobile element insertion2nstd211human GRCh38 chr15: 80,413,086-80,413,086 , GRCh37.p13 chr15: 80,705,428-80,705,428 ARNT2
    nsv5662153insertion1nstd207human GRCh38 chr15: 80,593,768-80,593,768 , GRCh37.p13 chr15: 80,886,109-80,886,109 ARNT2
    nsv5652481insertion1nstd207human GRCh38 chr15: 80,566,218-80,566,218 , GRCh37.p13 chr15: 80,858,559-80,858,559 ARNT2
    nsv5551827insertion1nstd206human GRCh38 chr15: 80,481,990-80,482,026 , GRCh37.p13 chr15: 80,774,331-80,774,367 ARNT2
    nsv5547707insertion1nstd206human GRCh38 chr15: 80,426,087-80,426,109 , GRCh37.p13 chr15: 80,718,429-80,718,451 ARNT2
    nsv5525961copy number variation1nstd206human GRCh38 chr15: 80,409,342-80,409,584 , GRCh37.p13 chr15: 80,701,684-80,701,926 ARNT2
    nsv5518496copy number variation1nstd206human GRCh38 chr15: 80,430,831-80,430,925 , GRCh37.p13 chr15: 80,723,173-80,723,267 ARNT2
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