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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5685663mobile element insertion2nstd211human GRCh38 chr7: 121,331,506-121,331,506 , GRCh37.p13 chr7: 120,971,560-120,971,560 WNT16
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5407478mobile element insertion1nstd206human GRCh38 chr7: 121,331,506-121,331,557 , GRCh37.p13 chr7: 120,971,560-120,971,611 WNT16
    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
    nsv5111749mobile element insertion1nstd203human GRCh38 chr7: 121,331,506-121,331,506 , GRCh37.p13 chr7: 120,971,560-120,971,560 WNT16
    nsv5109500mobile element insertion1nstd203human GRCh38 chr7: 121,331,492-121,331,506 , GRCh37.p13 chr7: 120,971,546-120,971,560 WNT16
    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
    nsv4957982copy number variation1nstd200human GRCh38 chr7: 121,329,826-121,330,049 , GRCh37.p13 chr7: 120,969,880-120,970,103 WNT16
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    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
    nsv4524370copy number variation1nstd166human GRCh37.p13 chr7: 120,599,997-121,277,000 , GRCh38.p12 chr7: 120,959,943-121,636,946 ING3, RPL18P4, 9 more genes
    nsv4493563mobile element insertion1nstd166human GRCh37.p13 chr7: 120,971,539-120,971,539 , GRCh38.p12 chr7: 121,331,485-121,331,485 WNT16
    nsv4490279mobile element insertion1nstd166human GRCh37.p13 chr7: 120,971,546-120,971,546 , GRCh38.p12 chr7: 121,331,492-121,331,492 WNT16
    nsv4456742copy number variation1nstd102humanUncertain significance GRCh37 chr7: 120,818,380-121,033,193 , GRCh38.p12 chr7: 121,178,326-121,393,139 RNU6-517P, WNT16, 2 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
    nsv4342388sequence alteration1nstd166human GRCh37.p13 chr7: 120,967,880-120,969,109 , GRCh38.p12 chr7: 121,327,826-121,329,055 WNT16
    nsv4170848copy number variation1nstd166human GRCh37.p13 chr7: 120,969,178-120,969,742 , GRCh38.p12 chr7: 121,329,124-121,329,688 WNT16
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