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Items: 1 to 20 of 280

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6115895mobile element insertion1nstd186human GRCh37 chr15: 59,169,383-59,169,434 , GRCh38.p12 chr15: 58,877,184-58,877,235 SLTM
    nsv5979355insertion1nstd209human GRCh38 chr15: 58,877,171-58,877,171 , GRCh37.p13 chr15: 59,169,370-59,169,370 SLTM
    nsv5973408insertion1nstd209human GRCh38 chr15: 58,882,181-58,882,181 , GRCh37.p13 chr15: 59,174,380-59,174,380 SLTM
    nsv5936050copy number variation1nstd209human GRCh38 chr15: 58,927,940-58,927,992 , GRCh37.p13 chr15: 59,220,139-59,220,191 SLTM
    nsv5705920mobile element insertion2nstd211human GRCh38 chr15: 58,928,598-58,928,598 , GRCh37.p13 chr15: 59,220,797-59,220,797 SLTM
    nsv5702125mobile element insertion2nstd211human GRCh38 chr15: 58,911,583-58,911,583 , GRCh37.p13 chr15: 59,203,782-59,203,782 SLTM
    nsv5698840mobile element insertion1nstd211human GRCh38 chr15: 58,886,250-58,886,250 , GRCh37.p13 chr15: 59,178,449-59,178,449 SLTM
    nsv5696860mobile element insertion2nstd211human GRCh38 chr15: 58,877,184-58,877,184 , GRCh37.p13 chr15: 59,169,383-59,169,383 SLTM
    nsv5663853insertion1nstd207human GRCh38 chr15: 58,877,171-58,877,171 , GRCh37.p13 chr15: 59,169,370-59,169,370 SLTM
    nsv5561109sequence alteration1nstd206human GRCh38 chr15: 58,869,604-59,552,865 , GRCh37.p13 chr15: 59,161,803-59,845,064 MYO1E, RNF111, 14 more genes
    nsv5527371copy number variation1nstd206human GRCh38 chr15: 58,928,624-58,928,720 , GRCh37.p13 chr15: 59,220,823-59,220,919 SLTM
    nsv5526443copy number variation1nstd206human GRCh38 chr15: 58,922,521-58,922,588 , GRCh37.p13 chr15: 59,214,720-59,214,787 SLTM
    nsv5432624mobile element insertion1nstd206human GRCh38 chr15: 58,928,598-58,928,649 , GRCh37.p13 chr15: 59,220,797-59,220,848 SLTM
    nsv5426933mobile element insertion1nstd206human GRCh38 chr15: 58,877,184-58,877,235 , GRCh37.p13 chr15: 59,169,383-59,169,434 SLTM
    nsv5426241mobile element insertion1nstd206human GRCh38 chr15: 58,911,583-58,911,634 , GRCh37.p13 chr15: 59,203,782-59,203,833 SLTM
    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
    nsv5158926mobile element insertion1nstd203human GRCh38 chr15: 58,928,588-58,928,598 , GRCh37.p13 chr15: 59,220,787-59,220,797 SLTM
    nsv5157443mobile element insertion1nstd203human GRCh38 chr15: 58,877,184-58,877,184 , GRCh37.p13 chr15: 59,169,383-59,169,383 SLTM
    nsv5157145mobile element insertion1nstd203human GRCh38 chr15: 58,877,176-58,877,184 , GRCh37.p13 chr15: 59,169,375-59,169,383 SLTM
    nsv5156479mobile element insertion1nstd203human GRCh38 chr15: 58,928,585-58,928,594 , GRCh37.p13 chr15: 59,220,784-59,220,793 SLTM
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