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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5700525mobile element insertion1nstd211human GRCh38 chr7: 142,917,190-142,917,190 , GRCh37.p13 chr7|NW_003571040.1: 1,120,021-1,120,021 TRPV5
    nsv5698910mobile element insertion2nstd211human GRCh38 chr7: 142,906,967-142,906,967 , GRCh37.p13 chr7|NW_003571040.1: 1,109,793-1,109,793 TRPV5
    nsv5626215insertion1nstd207human GRCh38 chr7: 142,924,341-142,924,341 , GRCh37.p13 chr7: 142,621,440-142,621,440 TRPV5
    nsv5582772copy number variation1nstd207human GRCh38 chr7: 142,924,301-142,924,376 , GRCh37.p13 chr7: 142,621,401-142,621,472 TRPV5
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5487403copy number variation1nstd206human GRCh38 chr7: 142,924,264-142,924,362 , GRCh37.p13 chr7: 142,621,401-142,621,459 TRPV5
    nsv5405741mobile element insertion1nstd206human GRCh38 chr7: 142,906,967-142,907,018 , GRCh37.p13 chr7|NW_003571040.1: 1,109,793-1,109,844 TRPV5
    nsv5371313translocation1nstd200human GRCh38 chr7: 142,917,061-142,917,061 , GRCh38 chr7: 142,916,544-142,916,544 , GRCh37.p13 chr7|NW_003571040.1: 1,119,374-1,119,374 , GRCh37.p13 chr7|NW_003571040.1: 1,119,892-1,119,892 TRPV5
    nsv5242793copy number variation1nstd204human GRCh38.p13 chr7: 142,922,997-142,929,043 , GRCh37.p13 chr7: 142,621,401-142,626,138 TRPV5
    nsv5104117mobile element insertion1nstd203human GRCh38 chr7: 142,906,951-142,906,967 , GRCh37.p13 chr7|NW_003571040.1: 1,109,777-1,109,793 TRPV5
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4752305insertion1nstd199human GRCh37 chr7: 142,621,385-142,621,385 , GRCh38.p12 chr7: 142,924,214-142,924,214 , GRCh38.p12 chr7|NT_187562.1: 947,281-947,281 TRPV5
    nsv4726707insertion1nstd186human GRCh37 chr7: 142,604,117-142,604,117 , GRCh38.p12 chr7|NT_187562.1: 930,018-930,018 , GRCh38.p12 chr7: 142,906,951-142,906,951 TRPV5
    nsv4675620copy number variation1nstd102humanPathogenic GRCh37 chr7: 109,251,060-159,119,707 , GRCh38.p12 chr7: 109,611,003-159,327,017 RPL26P23, ST13P17, 887 more genes
    nsv4675615copy number variation1nstd102humanPathogenic GRCh37 chr7: 131,414,604-159,126,310 , GRCh38.p12 chr7: 131,729,845-159,333,620 ATG9B, OR10AC1, 603 more genes
    nsv4616623copy number variation1nstd183human GRCh37 chr7: 142,568,666-142,703,508 , GRCh38.p12 chr7: 142,870,913-143,006,421 , GRCh38.p12 chr7|NT_187562.1: 893,956-1,029,488 , EPHB6, 5 more genes
    nsv4605707copy number variation1nstd183human GRCh37 chr7: 142,568,740-142,707,516 , GRCh38.p12 chr7: 142,870,987-143,010,429 , GRCh38.p12 chr7|NT_187562.1: 894,030-1,033,496 , EPHB6, 5 more genes
    nsv4548901insertion1nstd166human GRCh37.p13 chr7: 142,604,117-142,604,117 , GRCh38.p12 chr7: 142,906,951-142,906,951 , GRCh38.p12 chr7|NT_187562.1: 930,018-930,018 TRPV5
    nsv4525104copy number variation1nstd166human GRCh37.p13 chr7: 141,933,998-142,707,100 , GRCh38.p12 chr7: 142,288,582-143,010,013 , GRCh38.p12 chr7|NT_187562.1: 196,078-914,081 , TRBJ2-6, 108 more genes
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