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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7061495inversion1nstd229human GRCh38 chr12: 107,014,490-109,497,170 , GRCh37.p13 chr12: 107,408,268-109,934,975 RPL17P38, RNU6-361P, 46 more genes
    nsv6936647copy number variation1nstd229human GRCh38 chr12: 109,087,324-109,098,613 , GRCh37.p13 chr12: 109,525,129-109,536,418 ALKBH2, UNG, 1 more genes
    nsv6935598copy number variation1nstd229human GRCh38 chr12: 109,043,689-109,046,100 , GRCh37.p13 chr12: 109,481,494-109,483,905 USP30
    nsv6931732copy number variation1nstd229human GRCh38 chr12: 108,914,683-113,697,537 , GRCh37.p13 chr12: 109,308,459-114,135,342 PTPN11, RPL31P49, 111 more genes
    nsv6928165copy number variation1nstd229human GRCh38 chr12: 109,031,701-109,033,700 , GRCh37.p13 chr12: 109,469,506-109,471,505 USP30
    nsv6927054copy number variation1nstd229human GRCh38 chr12: 109,024,501-109,030,100 , GRCh37.p13 chr12: 109,462,306-109,467,905 USP30
    nsv6922947copy number variation1nstd229human GRCh38 chr12: 108,490,015-109,627,369 , GRCh37.p13 chr12: 108,883,792-110,065,174 RNU4-32P, LOC105369968, 30 more genes
    nsv6919520copy number variation1nstd229human GRCh38 chr12: 109,022,095-109,024,361 , GRCh37.p13 chr12: 109,459,900-109,462,166 USP30
    nsv6918113copy number variation1nstd229human GRCh38 chr12: 109,063,696-109,158,615 , GRCh37.p13 chr12: 109,501,501-109,596,420 UNG, USP30, 3 more genes
    nsv6621489copy number variation1nstd224human GRCh37 chr12: 109,201,326-110,355,704 , GRCh38.p12 chr12: 108,807,550-109,917,899 FAM222A, MYO1H, 29 more genes
    nsv6594607inversion1nstd223human GRCh38 chr12: 109,023,288-109,023,754 , GRCh37.p13 chr12: 109,461,093-109,461,559 USP30
    nsv6589776inversion1nstd223human GRCh38 chr12: 109,066,530-109,067,139 , GRCh37.p13 chr12: 109,504,335-109,504,944 USP30
    nsv6587653inversion1nstd223human GRCh38 chr12: 109,027,966-109,031,478 , GRCh37.p13 chr12: 109,465,771-109,469,283 USP30
    nsv6584531inversion1nstd223human GRCh38 chr12: 109,050,238-109,051,289 , GRCh37.p13 chr12: 109,488,043-109,489,094 USP30-AS1, USP30
    nsv6493898copy number variation1nstd223human GRCh38 chr12: 109,024,400-109,025,821 , GRCh37.p13 chr12: 109,462,205-109,463,626 USP30
    nsv6487376copy number variation1nstd223human GRCh38 chr12: 109,044,656-109,048,698 , GRCh37.p13 chr12: 109,482,461-109,486,503 USP30
    nsv6487231copy number variation1nstd223human GRCh38 chr12: 109,046,875-109,051,371 , GRCh37.p13 chr12: 109,484,680-109,489,176 USP30, USP30-AS1
    nsv6485946copy number variation1nstd223human GRCh38 chr12: 109,085,248-109,086,578 , GRCh37.p13 chr12: 109,523,053-109,524,383 USP30, ALKBH2
    nsv6475609copy number variation1nstd223human GRCh38 chr12: 109,063,696-109,158,615 , GRCh37.p13 chr12: 109,501,501-109,596,420 USP30, LOC105369974, 3 more genes
    nsv6314095copy number variation1nstd102humanUncertain significance GRCh37 chr12: 109,470,903-109,573,425 , GRCh38.p12 chr12: 109,033,098-109,135,620 ALKBH2, ACACB, 5 more genes
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