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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
    nsv5676019mobile element insertion2nstd211human GRCh38 chr7: 120,827,135-120,827,135 , GRCh37.p13 chr7: 120,467,189-120,467,189 TSPAN12
    nsv5673843copy number variation1nstd102humanPathogenic GRCh37 chr7: 120,428,646-120,446,746 , GRCh38.p12 chr7: 120,788,592-120,806,692 TSPAN12
    nsv5565255copy number variation1nstd207human GRCh38 chr7: 120,799,527-120,799,588 , GRCh37.p13 chr7: 120,439,581-120,439,642 TSPAN12
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5410797mobile element insertion1nstd206human GRCh38 chr7: 120,827,135-120,827,186 , GRCh37.p13 chr7: 120,467,189-120,467,240 TSPAN12
    nsv5381759copy number variation1nstd102humanPathogenic GRCh37 chr7: 116,297,277-126,370,694 , GRCh38.p12 chr7: 116,657,223-126,730,640 TMEM229A, ST7-OT3, 110 more genes
    nsv5326600inversion1nstd204human GRCh37.p13 chr7: 97,320,865-141,491,704 , GRCh38.p13 chr7: 97,691,553-141,791,904 , ARF5, 752 more genes
    nsv5115530mobile element insertion1nstd203human GRCh38 chr7: 120,810,670-120,810,681 , GRCh37.p13 chr7: 120,450,724-120,450,735 TSPAN12
    nsv5110020mobile element insertion1nstd203human GRCh38 chr7: 120,827,122-120,827,135 , GRCh37.p13 chr7: 120,467,176-120,467,189 TSPAN12
    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
    nsv4683601copy number variation1nstd102humanPathogenic GRCh37 chr7: 120,496,752-120,496,817 , GRCh38.p12 chr7: 120,856,698-120,856,763 TSPAN12
    nsv4683123copy number variation1nstd102humanUncertain significance GRCh37 chr7: 120,372,957-120,480,163 , GRCh38.p12 chr7: 120,732,903-120,840,109 KCND2, TSPAN12
    nsv4683078copy number variation1nstd102humanUncertain significance GRCh37 chr7: 120,428,646-120,428,951 , GRCh38.p12 chr7: 120,788,592-120,788,897 TSPAN12
    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
    nsv4675322copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,617,406-123,217,914 , GRCh38.p12 chr7: 106,976,961-123,577,860 CBLL1-AS1, COMETT, 168 more genes
    nsv4618519copy number variation1nstd183human GRCh37 chr7: 120,392,929-120,444,391 , GRCh38.p12 chr7: 120,752,875-120,804,337 TSPAN12
    nsv4617443copy number variation1nstd183human GRCh37 chr7: 120,388,177-120,446,976 , GRCh38.p12 chr7: 120,748,123-120,806,922 KCND2, TSPAN12
    nsv4570752sequence alteration1nstd166human GRCh37.p13 chr7: 119,652,114-120,528,268 , GRCh38.p12 chr7: 120,012,060-120,888,214 KCND2, TSPAN12, 2 more genes
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