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Items: 1 to 20 of 581

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7093966copy number variation1nstd102humanUncertain significance GRCh37 chr12: 20,522,219-22,089,608 , GRCh38.p12 chr12: 20,369,285-21,936,674 LOC728688, SPX, 19 more genes
    nsv7077690inversion1nstd229human GRCh38 chr12: 21,127,821-21,448,917 , GRCh37.p13 chr12: 21,280,755-21,601,851 SLCO1A2, SLCO1B1, 3 more genes
    nsv7076490inversion1nstd229human GRCh38 chr12: 20,940,376-25,948,754 , GRCh37.p13 chr12: 21,093,310-26,101,687 LOC102724261, IRAG2, 59 more genes
    nsv7073166inversion1nstd229human GRCh38 chr12: 21,291,027-21,291,039 , GRCh37.p13 chr12: 21,443,961-21,443,973 SLCO1A2
    nsv7072461inversion1nstd229human GRCh38 chr12: 21,060,700-21,582,859 , GRCh37.p13 chr12: 21,213,634-21,735,793 RECQL, SLCO1B1, 9 more genes
    nsv7072309inversion1nstd229human GRCh38 chr12: 20,907,972-21,582,861 , GRCh37.p13 chr12: 21,060,906-21,735,795 RECQL, SLCO1B1, 10 more genes
    nsv7070569inversion1nstd229human GRCh38 chr12: 21,394,707-21,415,177 , GRCh37.p13 chr12: 21,547,641-21,568,111 SLCO1A2
    nsv7070485inversion1nstd229human GRCh38 chr12: 21,009,516-22,041,867 , GRCh37.p13 chr12: 21,162,450-22,194,801 SLCO1B3-SLCO1B7, SPX, 15 more genes
    nsv7068678inversion1nstd229human GRCh38 chr12: 20,996,324-22,051,286 , GRCh37.p13 chr12: 21,149,258-22,204,220 SLCO1B3-SLCO1B7, ABCC9, 16 more genes
    nsv7068185inversion1nstd229human GRCh38 chr12: 20,036,076-21,999,484 , GRCh37.p13 chr12: 20,189,010-22,152,418 UBE2L2, RECQL, 25 more genes
    nsv7064660inversion1nstd229human GRCh38 chr12: 21,238,037-21,424,101 , GRCh37.p13 chr12: 21,390,971-21,577,035 IAPP, SLCO1A2, 1 more genes
    nsv7063671inversion1nstd229human GRCh38 chr12: 20,030,237-21,994,711 , GRCh37.p13 chr12: 20,183,171-22,147,645 SLCO1B3-SLCO1B7, LINC02468, 25 more genes
    nsv7061480inversion1nstd229human GRCh38 chr12: 21,215,072-21,382,982 , GRCh37.p13 chr12: 21,368,006-21,535,916 SLCO1A2, SLCO1B1, 1 more genes
    nsv7060644inversion1nstd229human GRCh38 chr12: 20,030,249-21,999,483 , GRCh37.p13 chr12: 20,183,183-22,152,417 SLCO1B3-SLCO1B7, SLCO1B3, 25 more genes
    nsv7058718inversion1nstd229human GRCh38 chr12: 21,332,954-21,340,146 , GRCh37.p13 chr12: 21,485,888-21,493,080 SLCO1A2
    nsv6935668copy number variation1nstd229human GRCh38 chr12: 21,353,644-21,361,899 , GRCh37.p13 chr12: 21,506,578-21,514,833 IAPP, SLCO1A2
    nsv6933872copy number variation1nstd229human GRCh38 chr12: 21,341,977-21,342,185 , GRCh37.p13 chr12: 21,494,911-21,495,119 SLCO1A2
    nsv6933207copy number variation1nstd229human GRCh38 chr12: 21,344,766-21,349,376 , GRCh37.p13 chr12: 21,497,700-21,502,310 SLCO1A2
    nsv6932571copy number variation1nstd229human GRCh38 chr12: 21,374,613-21,389,941 , GRCh37.p13 chr12: 21,527,547-21,542,875 IAPP, SLCO1A2
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