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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5907808copy number variation1nstd209human GRCh38 chr7: 129,160,268-129,160,337 , GRCh37.p13 chr7: 128,800,109-128,800,178 TSPAN33
    nsv5713461mobile element insertion2nstd211human GRCh38 chr7: 129,147,173-129,147,173 , GRCh37.p13 chr7: 128,787,014-128,787,014 TSPAN33
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5534886insertion1nstd206human GRCh38 chr7: 129,144,727-129,144,741 , GRCh37.p13 chr: NaN-NaN TSPAN33
    nsv5407186mobile element insertion1nstd206human GRCh38 chr7: 129,147,173-129,147,224 , GRCh37.p13 chr7: 128,787,014-128,787,065 TSPAN33
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    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
    nsv4768707insertion1nstd186human GRCh37 chr7: 128,784,712-128,784,712 , GRCh38.p12 chr7: 129,144,658-129,144,658 TSPAN33
    nsv4763299insertion1nstd199human GRCh37 chr7: 128,784,713-128,784,713 , GRCh38.p12 chr7: 129,144,659-129,144,659 TSPAN33
    nsv4684479insertion1nstd194human GRCh37 chr7: 128,784,712-128,784,712 , GRCh38.p12 chr7: 129,144,658-129,144,658 TSPAN33
    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
    nsv4487543mobile element insertion1nstd166human GRCh37.p13 chr7: 128,786,998-128,786,998 , GRCh38.p12 chr7: 129,147,157-129,147,157 TSPAN33
    nsv4479024mobile element insertion1nstd166human GRCh37.p13 chr7: 128,797,371-128,797,371 , GRCh38.p12 chr7: 129,157,530-129,157,530 TSPAN33
    nsv4455826copy number variation1nstd102humanPathogenic GRCh37 chr7: 121,480,906-129,389,003 , GRCh38.p12 chr7: 121,840,852-129,749,163 ASB15, PNPT1P2, 127 more genes
    nsv4455091copy number variation1nstd102humanPathogenic GRCh37 chr7: 10,365-159,119,707 , GRCh38.p12 chr7: 10,365-159,327,017 RPL23AP51, FLJ40288, 2684 more genes
    nsv4446959insertion1nstd175human GRCh37 chr7: 128,784,711-128,784,711 , GRCh38.p12 chr7: 129,144,657-129,144,657 TSPAN33
    nsv4349183copy number variation1nstd102humanPathogenic GRCh37 chr7: 128,312,450-159,119,220 , GRCh38.p12 chr7: 128,672,396-159,326,530 LOC105375582, TRBJ2-4, 686 more genes
    nsv4322564inversion1nstd166human GRCh37.p13 chr7: 125,283,973-130,824,546 , GRCh38.p12 chr7: 125,643,919-131,139,787 , ARF5, 119 more genes
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