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Items: 1 to 20 of 240

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129406insertion1nstd186human GRCh37 chr15: 63,882,045-63,882,051 , GRCh38.p12 chr15: 63,589,846-63,589,852 USP3, USP3-AS1
    nsv5977070insertion1nstd209human GRCh38 chr15: 63,589,847-63,589,847 , GRCh37.p13 chr15: 63,882,046-63,882,046 USP3, USP3-AS1
    nsv5969978insertion1nstd209human GRCh38 chr15: 63,547,888-63,547,888 , GRCh37.p13 chr15: 63,840,087-63,840,087 USP3
    nsv5940560copy number variation1nstd209human GRCh38 chr15: 63,548,002-63,548,260 , GRCh37.p13 chr15: 63,840,201-63,840,459 USP3
    nsv5704991mobile element insertion1nstd211human GRCh38 chr15: 63,553,867-63,553,867 , GRCh37.p13 chr15: 63,846,066-63,846,066 USP3
    nsv5704505mobile element insertion1nstd211human GRCh38 chr15: 63,549,038-63,549,038 , GRCh37.p13 chr15: 63,841,237-63,841,237 USP3
    nsv5696768mobile element insertion1nstd211human GRCh38 chr15: 63,506,745-63,506,745 , GRCh37.p13 chr15: 63,798,944-63,798,944 USP3
    nsv5655937insertion1nstd207human GRCh38 chr15: 63,589,845-63,589,845 , GRCh37.p13 chr15: 63,882,044-63,882,044 USP3-AS1, USP3
    nsv5596624copy number variation1nstd207human GRCh38 chr15: 63,547,722-63,547,771 , GRCh37.p13 chr15: 63,839,921-63,839,970 USP3
    nsv5543369insertion1nstd206human GRCh38 chr15: 63,589,846-63,589,852 , GRCh37.p13 chr15: 63,882,045-63,882,051 USP3, USP3-AS1
    nsv5532556copy number variation1nstd206human GRCh38 chr15: 63,555,327-63,555,394 , GRCh37.p13 chr15: 63,847,526-63,847,593 USP3
    nsv5526062copy number variation1nstd206human GRCh38 chr15: 63,576,763-63,576,902 , GRCh37.p13 chr15: 63,868,962-63,869,101 USP3
    nsv5419554mobile element insertion1nstd206human GRCh38 chr15: 63,506,745-63,506,796 , GRCh37.p13 chr15: 63,798,944-63,798,995 USP3
    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
    nsv5379604translocation1nstd200human GRCh38 chr12: 26,784,453-26,784,453 , GRCh38 chr15: 63,561,718-63,561,718 , GRCh37.p13 chr12: 26,937,386-26,937,386 , GRCh37.p13 chr15: 63,853,917-63,853,917 , ITPR2, 1 more genes
    nsv5335577translocation1nstd200human GRCh37 chr15: 63,797,194-63,797,194 , GRCh37 chr15: 63,797,375-63,797,375 , GRCh38.p12 chr15: 63,504,995-63,504,995 , GRCh38.p12 chr15: 63,505,176-63,505,176 USP3
    nsv5159549mobile element insertion1nstd203human GRCh38 chr15: 63,531,329-63,531,341 , GRCh37.p13 chr15: 63,823,528-63,823,540 USP3
    nsv5146955mobile element insertion1nstd203human GRCh38 chr15: 63,549,027-63,549,038 , GRCh37.p13 chr15: 63,841,226-63,841,237 USP3
    nsv5143903mobile element insertion1nstd203human GRCh38 chr15: 63,549,032-63,549,038 , GRCh37.p13 chr15: 63,841,231-63,841,237 USP3
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
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