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Items: 1 to 20 of 226

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144230insertion1nstd232human GRCh37.p13 chr15: 52,245,462-52,245,462 , GRCh38.p12 chr15: 51,953,265-51,953,265 LEO1
    nsv7094385copy number variation2nstd102humanPathogenic GRCh37 chr15: 50,999,997-54,025,330 , GRCh38.p12 chr15: 50,707,800-53,733,133 LOC105370826, MIR7973-2, 48 more genes
    nsv7094384copy number variation1nstd102humanUncertain significance GRCh37 chr15: 50,731,271-54,025,330 , GRCh38.p12 chr15: 50,439,074-53,733,133 LOC105370823, TMOD3, 54 more genes
    nsv7059635inversion1nstd229human GRCh38 chr15: 51,716,761-55,548,818 , GRCh37.p13 chr15: 52,008,958-55,841,016 CCPG1, LOC105370823, 51 more genes
    nsv7059534inversion1nstd229human GRCh38 chr15: 51,726,660-55,605,328 , GRCh37.p13 chr15: 52,018,857-55,897,526 HNRNPA1P74, MYO5C, 50 more genes
    nsv6978065copy number variation1nstd229human GRCh38 chr15: 51,918,137-51,972,410 , GRCh37.p13 chr15: 52,210,334-52,264,607 LOC100422556, LOC112268148, 1 more genes
    nsv6977993copy number variation1nstd229human GRCh38 chr15: 51,773,555-52,058,797 , GRCh37.p13 chr15: 52,065,752-52,350,994 TMOD2, LEO1, 8 more genes
    nsv6974455copy number variation1nstd229human GRCh38 chr15: 51,938,906-51,938,959 , GRCh37.p13 chr15: 52,231,103-52,231,156 LEO1, LOC112268148
    nsv6972493copy number variation1nstd229human GRCh38 chr15: 51,971,701-51,981,400 , GRCh37.p13 chr15: 52,263,898-52,273,597 LEO1
    nsv6964655copy number variation1nstd229human GRCh38 chr15: 51,971,301-51,981,500 , GRCh37.p13 chr15: 52,263,498-52,273,697 LEO1
    nsv6962875copy number variation1nstd229human GRCh38 chr15: 51,967,123-51,968,042 , GRCh37.p13 chr15: 52,259,320-52,260,239 LEO1
    nsv6962666copy number variation1nstd229human GRCh38 chr15: 51,941,811-51,946,997 , GRCh37.p13 chr15: 52,234,008-52,239,194 LOC112268148, LEO1
    nsv6958330copy number variation1nstd229human GRCh38 chr15: 51,971,101-51,981,500 , GRCh37.p13 chr15: 52,263,298-52,273,697 LEO1
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
    nsv6594587inversion1nstd223human GRCh38 chr15: 51,961,180-51,961,556 , GRCh37.p13 chr15: 52,253,377-52,253,753 LEO1
    nsv6511431copy number variation1nstd223human GRCh38 chr15: 51,941,811-51,946,991 , GRCh37.p13 chr15: 52,234,008-52,239,188 LOC112268148, LEO1
    nsv6505222copy number variation1nstd223human GRCh38 chr15: 51,932,166-52,011,423 , GRCh37.p13 chr15: 52,224,363-52,303,620 MAPK6-DT, LOC112268148, 1 more genes
    nsv6504463copy number variation1nstd223human GRCh38 chr15: 51,929,778-51,936,966 , GRCh37.p13 chr15: 52,221,975-52,229,163 LOC112268148, LEO1
    nsv6502905copy number variation1nstd223human GRCh38 chr15: 51,971,301-51,981,500 , GRCh37.p13 chr15: 52,263,498-52,273,697 LEO1
    nsv6497327copy number variation1nstd223human GRCh38 chr15: 51,964,071-52,025,722 , GRCh37.p13 chr15: 52,256,268-52,317,919 MAPK6, MAPK6-DT, 1 more genes
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