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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5947947insertion1nstd209human GRCh38 chr7: 121,371,585-121,371,585 , GRCh37.p13 chr7: 121,011,639-121,011,639 FAM3C
    nsv5916601copy number variation1nstd209human GRCh38 chr7: 121,366,345-121,366,396 , GRCh37.p13 chr7: 121,006,399-121,006,450 FAM3C
    nsv5692664mobile element insertion1nstd211human GRCh38 chr7: 121,386,955-121,386,955 , GRCh37.p13 chr7: 121,027,009-121,027,009 FAM3C
    nsv5628875insertion1nstd207human GRCh38 chr7: 121,395,234-121,395,234 , GRCh37.p13 chr7: 121,035,288-121,035,288 FAM3C
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5493905copy number variation1nstd206human GRCh38 chr7: 121,366,346-121,366,397 , GRCh37.p13 chr7: 121,006,400-121,006,451 FAM3C
    nsv5490688copy number variation1nstd206human GRCh38 chr7: 121,357,510-121,358,357 , GRCh37.p13 chr7: 120,997,564-120,998,411 FAM3C
    nsv5475862copy number variation1nstd206human GRCh38 chr7: 121,383,055-121,383,119 , GRCh37.p13 chr7: 121,023,109-121,023,173 FAM3C
    nsv5475041copy number variation1nstd206human GRCh38 chr7: 121,347,606-121,349,168 , GRCh37.p13 chr7: 120,987,660-120,989,222 FAM3C
    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
    nsv5117056mobile element insertion1nstd203human GRCh38 chr7: 121,359,371-121,359,383 , GRCh37.p13 chr7: 120,999,425-120,999,437 FAM3C
    nsv5112192mobile element insertion1nstd203human GRCh38 chr7: 121,386,942-121,386,955 , GRCh37.p13 chr7: 121,026,996-121,027,009 FAM3C
    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
    nsv4957983copy number variation1nstd200human GRCh38 chr7: 121,382,541-121,386,638 , GRCh37.p13 chr7: 121,022,595-121,026,692 FAM3C
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4825304copy number variation1nstd200human GRCh37 chr7: 120,997,564-120,998,411 , GRCh38.p12 chr7: 121,357,510-121,358,357 FAM3C
    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
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