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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116526mobile element insertion1nstd186human GRCh37 chr15: 72,639,537-72,639,537 , GRCh38.p12 chr15: 72,347,196-72,347,196 HEXA
    nsv5972641insertion1nstd209human GRCh38 chr15: 72,347,196-72,347,196 , GRCh37.p13 chr15: 72,639,537-72,639,537 HEXA
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5696477mobile element insertion2nstd211human GRCh38 chr15: 72,347,210-72,347,210 , GRCh37.p13 chr15: 72,639,551-72,639,551 HEXA
    nsv5672589copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 72,637,767-72,639,071 , GRCh38.p12 chr15: 72,345,426-72,346,730 HEXA
    nsv5653729insertion1nstd207human GRCh38 chr15: 72,347,196-72,347,196 , GRCh37.p13 chr15: 72,639,537-72,639,537 HEXA
    nsv5525043copy number variation1nstd206human GRCh38 chr15: 72,366,954-72,368,780 , GRCh37.p13 chr15: 72,659,295-72,661,121 HEXA
    nsv5425827mobile element insertion1nstd206human GRCh38 chr15: 72,347,196-72,347,196 , GRCh37.p13 chr15: 72,639,537-72,639,537 HEXA
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5349149translocation1nstd200human GRCh38 chr15: 72,367,355-72,367,355 , GRCh38 chr15: 72,361,440-72,361,440 , GRCh37.p13 chr15: 72,653,781-72,653,781 , GRCh37.p13 chr15: 72,659,696-72,659,696 HEXA
    nsv5184491mobile element insertion1nstd203human GRCh38 chr15: 72,362,955-72,362,970 , GRCh37.p13 chr15: 72,655,296-72,655,311 HEXA
    nsv5159968mobile element insertion1nstd203human GRCh38 chr15: 72,347,199-72,347,210 , GRCh37.p13 chr15: 72,639,540-72,639,551 HEXA
    nsv5157413mobile element insertion1nstd203human GRCh38 chr15: 72,347,202-72,347,210 , GRCh37.p13 chr15: 72,639,543-72,639,551 HEXA
    nsv5157392mobile element insertion1nstd203human GRCh38 chr15: 72,347,194-72,347,210 , GRCh37.p13 chr15: 72,639,535-72,639,551 HEXA
    nsv5157257mobile element insertion1nstd203human GRCh38 chr15: 72,347,195-72,347,210 , GRCh37.p13 chr15: 72,639,536-72,639,551 HEXA
    nsv5155826mobile element insertion1nstd203human GRCh38 chr15: 72,347,203-72,347,210 , GRCh37.p13 chr15: 72,639,544-72,639,551 HEXA
    nsv5152857mobile element insertion1nstd203human GRCh38 chr15: 72,347,196-72,347,210 , GRCh37.p13 chr15: 72,639,537-72,639,551 HEXA
    nsv5151375mobile element insertion1nstd203human GRCh38 chr15: 72,347,197-72,347,208 , GRCh37.p13 chr15: 72,639,538-72,639,549 HEXA
    nsv5149718mobile element insertion1nstd203human GRCh38 chr15: 72,347,198-72,347,210 , GRCh37.p13 chr15: 72,639,539-72,639,551 HEXA
    nsv5148248mobile element insertion1nstd203human GRCh38 chr15: 72,347,484-72,347,531 , GRCh37.p13 chr15: 72,639,825-72,639,872 HEXA
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