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Items: 1 to 20 of 157

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7043557inversion1nstd229human GRCh38 chr7: 121,068,177-121,448,653 , GRCh37.p13 chr7: 120,708,231-121,088,707 WNT16, FAM3C, 5 more genes
    nsv6836474copy number variation1nstd229human GRCh38 chr7: 121,218,276-121,383,393 , GRCh37.p13 chr7: 120,858,330-121,023,447 WNT16, FAM3C, 1 more genes
    nsv6829033copy number variation1nstd229human GRCh38 chr7: 121,177,636-121,398,527 , GRCh37.p13 chr7: 120,817,690-121,038,581 CPED1, WNT16, 3 more genes
    nsv6825744copy number variation1nstd229human GRCh38 chr7: 120,119,180-121,466,883 , GRCh37.p13 chr7: 119,759,234-121,106,937 WNT16, CYCSP19, 12 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6631755copy number variation1nstd224human GRCh37 chr7: 120,822,386-121,046,807 , GRCh38.p12 chr7: 121,182,332-121,406,753 FAM3C, CYCSP19, 3 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6314995copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 114,885,745-124,728,629 , GRCh38.p12 chr7: 115,245,691-125,088,575 CAPZA2, CAV1, 109 more genes
    nsv6313851copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,984,287-128,949,489 , GRCh38.p12 chr7: 107,343,842-129,309,648 DOCK4-AS1, RPL3P8, 262 more genes
    nsv6290807copy number variation1nstd102humanUncertain significance GRCh37 chr7: 120,813,156-121,033,289 , GRCh38.p12 chr7: 121,173,102-121,393,235 FAM3C, RNU6-517P, 2 more genes
    nsv6239648mobile element insertion1nstd215human GRCh38 chr7: 121,331,506-121,331,506 , GRCh37.p13 chr7: 120,971,560-120,971,560 WNT16
    nsv6136546copy number variation1nstd213human GRCh37 chr7: 120,110,000-126,120,001 , GRCh38.p12 chr7: 120,469,946-126,479,947 SSU72L6, IQUB, 67 more genes
    nsv6135880copy number variation1nstd213human GRCh37 chr7: 119,540,000-121,050,001 , GRCh38.p12 chr7: 119,899,946-121,409,947 KCND2, FAM3C, 13 more genes
    nsv6135872copy number variation1nstd213human GRCh37 chr7: 113,230,000-128,010,001 , GRCh38.p12 chr7: 113,589,945-128,369,947 CAV1, SLC13A1, 154 more genes
    nsv6135545copy number variation1nstd213human GRCh37 chr7: 117,870,000-125,940,001 , GRCh38.p12 chr7: 118,229,946-126,299,947 GPR37, KCND2, 78 more genes
    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
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