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Items: 1 to 20 of 111

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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
    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
    nsv6929984copy number variation1nstd229human GRCh38 chr12: 109,088,690-109,088,803 , GRCh37.p13 chr12: 109,526,495-109,526,608 ALKBH2
    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
    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
    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
    nsv6291583copy number variation1nstd102humanPathogenic GRCh37 chr12: 104,230,462-111,984,801 , GRCh38.p12 chr12: 103,836,684-111,546,997 LOC105369964, LOC644746, 147 more genes
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132406copy number variation1nstd213human GRCh37 chr12: 108,420,000-110,500,001 , GRCh38.p12 chr12: 108,026,223-110,062,196 DAO, SART3, 47 more genes
    nsv5932661copy number variation1nstd209human GRCh38 chr12: 109,090,575-109,090,682 , GRCh37.p13 chr12: 109,528,380-109,528,487 ALKBH2
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv4993660copy number variation1nstd200human GRCh38 chr12: 109,063,696-109,158,618 , GRCh37.p13 chr12: 109,501,501-109,596,423 ALKBH2, LOC105369974, 3 more genes
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4835223copy number variation1nstd200human GRCh37 chr12: 109,501,500-109,596,424 , GRCh38.p12 chr12: 109,063,695-109,158,619 ACACB, USP30, 3 more genes
    nsv4769383copy number variation1nstd102humanUncertain significance GRCh37 chr12: 107,197,584-109,830,564 , GRCh38.p12 chr12: 106,803,806-109,392,759 TMEM263, MYO1H, 50 more genes
    nsv4756208inversion1nstd199human GRCh37 chr12: 104,359,633-125,801,147 , GRCh38.p12 chr12: 103,965,855-125,316,601 , ACACB, 453 more genes
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