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Items: 1 to 20 of 402

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6113760mobile element insertion1nstd186human GRCh37 chr3: 115,383,091-115,383,142 , GRCh38.p12 chr3: 115,664,244-115,664,295 GAP43
    nsv5966325insertion1nstd209human GRCh38 chr3: 115,664,230-115,664,230 , GRCh37.p13 chr3: 115,383,077-115,383,077 GAP43
    nsv5965685insertion1nstd209human GRCh38 chr3: 115,698,287-115,698,287 , GRCh37.p13 chr3: 115,417,134-115,417,134 GAP43
    nsv5888217copy number variation1nstd209human GRCh38 chr3: 115,631,022-115,631,351 , GRCh37.p13 chr3: 115,349,869-115,350,198 GAP43
    nsv5834288copy number variation1nstd209human GRCh38 chr3: 115,715,015-115,717,287 , GRCh37.p13 chr3: 115,433,862-115,436,134 GAP43
    nsv5691503mobile element insertion2nstd211human GRCh38 chr3: 115,661,845-115,661,845 , GRCh37.p13 chr3: 115,380,692-115,380,692 GAP43
    nsv5691422mobile element insertion2nstd211human GRCh38 chr3: 115,664,244-115,664,244 , GRCh37.p13 chr3: 115,383,091-115,383,091 GAP43
    nsv5681047mobile element insertion2nstd211human GRCh38 chr3: 115,645,795-115,645,795 , GRCh37.p13 chr3: 115,364,642-115,364,642 GAP43
    nsv5623442insertion1nstd207human GRCh38 chr3: 115,664,230-115,664,230 , GRCh37.p13 chr3: 115,383,077-115,383,077 GAP43
    nsv5622254insertion1nstd207human GRCh38 chr3: 115,698,281-115,698,281 , GRCh37.p13 chr3: 115,417,128-115,417,128 GAP43
    nsv5621686insertion1nstd207human GRCh38 chr3: 115,698,074-115,698,074 , GRCh37.p13 chr3: 115,416,921-115,416,921 GAP43
    nsv5449627copy number variation1nstd206human GRCh38 chr3: 115,698,065-115,698,123 , GRCh37.p13 chr3: 115,416,912-115,416,970 GAP43
    nsv5440406copy number variation1nstd206human GRCh38 chr3: 115,651,330-115,651,402 , GRCh37.p13 chr3: 115,370,177-115,370,249 GAP43
    nsv5440208copy number variation1nstd206human GRCh38 chr3: 115,635,740-115,637,772 , GRCh37.p13 chr3: 115,354,587-115,356,619 GAP43
    nsv5439990copy number variation1nstd206human GRCh38 chr3: 115,652,323-115,652,397 , GRCh37.p13 chr3: 115,371,170-115,371,244 GAP43
    nsv5435924copy number variation1nstd206human GRCh38 chr3: 115,635,206-115,635,556 , GRCh37.p13 chr3: 115,354,053-115,354,403 GAP43
    nsv5403839mobile element insertion1nstd206human GRCh38 chr3: 115,645,795-115,645,846 , GRCh37.p13 chr3: 115,364,642-115,364,693 GAP43
    nsv5402487mobile element insertion1nstd206human GRCh38 chr3: 115,664,244-115,664,295 , GRCh37.p13 chr3: 115,383,091-115,383,142 GAP43
    nsv5346436translocation1nstd200human GRCh38 chr3: 115,637,772-115,637,772 , GRCh38 chr3: 115,635,740-115,635,740 , GRCh37.p13 chr3: 115,356,619-115,356,619 , GRCh37.p13 chr3: 115,354,587-115,354,587 GAP43
    nsv5341340translocation1nstd200human GRCh37 chr3: 115,371,170-115,371,170 , GRCh37 chr3: 115,371,244-115,371,244 , GRCh38.p12 chr3: 115,652,397-115,652,397 , GRCh38.p12 chr3: 115,652,323-115,652,323 GAP43
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