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Items: 1 to 20 of 170

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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
    nsv7094215copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,479,509-4,488,748 , GRCh38.p12 chr12: 4,370,343-4,379,582 FGF23
    nsv7094213copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-4,796,274 , GRCh38.p12 chr12: 4,259,186-4,687,108 RPS15P7, RAD51AP1, 11 more genes
    nsv7094047copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-9,027,607 , GRCh38.p12 chr12: 4,259,186-8,875,011 ACRBP, OR7E148P, 165 more genes
    nsv7094046copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-5,155,155 , GRCh38.p12 chr12: 4,259,186-5,045,989 RPS15P7, CCND2, 18 more genes
    nsv7072221inversion1nstd229human GRCh38 chr12: 4,055,290-11,695,188 , GRCh37.p13 chr12: 4,164,456-11,848,122 RN7SL69P, KLRA1P, 285 more genes
    nsv7068624inversion1nstd229human GRCh38 chr12: 2,500,360-5,372,895 , GRCh37.p13 chr12: 2,609,526-5,482,061 LOC105369607, IQSEC3P1, 62 more genes
    nsv6931013copy number variation1nstd229human GRCh38 chr12: 4,335,593-4,573,659 , GRCh37.p13 chr12: 4,444,759-4,682,825 TIGAR, FGF6, 4 more genes
    nsv6918545copy number variation1nstd229human GRCh38 chr12: 4,366,569-4,399,823 , GRCh37.p13 chr12: 4,475,735-4,508,989 FGF23
    nsv6913746copy number variation1nstd229human GRCh38 chr12: 3,972,756-5,647,610 , GRCh37.p13 chr12: 4,081,922-5,756,776 LOC101901829, LOC100420673, 29 more genes
    nsv6637376copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,787-8,320,544 , GRCh38.p12 chr12: 64,621-8,167,948 GCSHP4, RNU7-1, 220 more genes
    nsv6473617copy number variation1nstd223human GRCh38 chr12: 3,972,756-5,647,610 , GRCh37.p13 chr12: 4,081,922-5,756,776 KCNA5, LINC02443, 29 more genes
    nsv6313933copy number variation1nstd102humanPathogenic GRCh37 chr12: 2,790,077-5,325,700 , GRCh38.p12 chr12: 2,680,911-5,216,534 OTUD4P1, DYRK4, 59 more genes
    nsv6309478copy number variation1nstd102humanUncertain significance GRCh37 chr12: 4,368,352-4,479,969 , GRCh38.p12 chr12: 4,259,186-4,370,803 CCND2, CCND2-AS1, 3 more genes
    nsv6290254copy number variation1nstd102humanPathogenic GRCh37 chr12: 146,240-8,330,229 , GRCh38.p12 chr12: 45,740-8,177,633 CLEC4A, FBXL14, 220 more genes
    nsv6132693copy number variation1nstd213human GRCh37 chr12: 3,310,000-5,630,001 , GRCh38.p12 chr12: 3,200,834-5,520,835 CCND2, FGF6, 44 more genes
    nsv6132422copy number variation1nstd213human GRCh37 chr12: 190,000-30,830,001 , GRCh38.p12 chr12: 80,834-30,677,067 , A2M, 622 more genes
    nsv6132246copy number variation1nstd213human GRCh37 chr12: 4,460,000-4,700,001 , GRCh38.p12 chr12: 4,350,834-4,590,835 FGF6, FGF23, 4 more genes
    nsv6112763copy number variation1nstd102humanPathogenic GRCh37 chr12: 189,145-7,730,395 , GRCh38.p12 chr12: 79,979-7,577,799 GALNT8, LINC02371, 197 more genes
    nsv6112730copy number variation1nstd102humanPathogenic GRCh37 chr12: 4,477,393-4,488,878 , GRCh38.p12 chr12: 4,368,227-4,379,712 FGF23
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