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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047961inversion1nstd229human GRCh38 chr7: 123,155,784-130,261,366 , GRCh37.p13 chr7: 122,795,838-129,901,206 IQUB, LOC107986843, 122 more genes
    nsv7047247inversion1nstd229human GRCh38 chr7: 123,130,391-130,261,365 , GRCh37.p13 chr7: 122,770,445-129,901,205 RNA5SP244, RNA5SP243, 122 more genes
    nsv7043190inversion1nstd229human GRCh38 chr7: 123,472,699-130,834,800 , GRCh37.p13 chr7: 123,112,753-129,984,423 KCP, LINC01000, 138 more genes
    nsv6824517copy number variation1nstd229human GRCh38 chr7: 123,313,906-124,175,429 , GRCh37.p13 chr7: 122,953,960-123,815,483 TMEM229A, LOC105375483, 11 more genes
    nsv6823622copy number variation1nstd229human GRCh38 chr7: 123,815,605-123,815,811 , GRCh37.p13 chr7: 123,455,659-123,455,865 HYAL4, HYAL6P
    nsv6819445copy number variation1nstd229human GRCh38 chr7: 123,815,221-123,835,480 , GRCh37.p13 chr7: 123,455,275-123,475,534 HYAL4, HYAL6P
    nsv6818132copy number variation1nstd229human GRCh38 chr7: 123,702,601-123,824,400 , GRCh37.p13 chr7: 123,342,655-123,464,454 HYAL4, RNU6-11P, 2 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
    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
    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
    nsv6135886copy number variation1nstd213human GRCh37 chr7: 123,360,000-123,710,001 , GRCh38.p12 chr7: 123,719,946-124,069,947 SPAM1, WASL, 5 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
    nsv5632587insertion1nstd207human GRCh38 chr7: 123,817,784-123,817,784 , GRCh37.p13 chr7: 123,457,838-123,457,838 HYAL6P, HYAL4
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5475613copy number variation1nstd206human GRCh38 chr7: 123,815,221-123,835,480 , GRCh37.p13 chr7: 123,455,275-123,475,534 HYAL6P, HYAL4
    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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