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Items: 1 to 20 of 182

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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
    nsv7071757inversion1nstd229human GRCh38 chr12: 2,390,179-3,608,024 , GRCh37.p13 chr12: 2,499,345-3,717,190 THCAT155, TSPAN9, 28 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
    nsv6908371copy number variation1nstd229human GRCh38 chr12: 3,061,035-3,743,985 , GRCh37.p13 chr12: 3,170,201-3,853,151 PRMT8, LOC105369607, 11 more genes
    nsv6637408copy number variation1nstd102humanUncertain significance GRCh37 chr12: 3,282,099-3,845,523 , GRCh38.p12 chr12: 3,172,933-3,736,357 PRMT8, LOC105369607, 10 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
    nsv6467392copy number variation1nstd223human GRCh38 chr12: 3,272,176-3,485,681 , GRCh37.p13 chr12: 3,381,342-3,594,847 LINC02827, THCAT155, 7 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
    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
    nsv6132329copy number variation1nstd213human GRCh37 chr12: 190,000-3,760,001 , GRCh38.p12 chr12: 80,834-3,650,835 TEAD4, NRIP2, 73 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
    nsv5921920copy number variation1nstd209human GRCh38 chr12: 3,058,695-6,171,259 , GRCh37.p13 chr12: 3,167,861-6,280,425 , LOC105369623, 54 more genes
    nsv4729176copy number variation1nstd102humanPathogenic GRCh37 chr12: 191,242-4,683,495 , GRCh38.p12 chr12: 82,076-4,574,329 RPL18P9, CACNA1C, 92 more genes
    nsv4729021copy number variation1nstd102humanUncertain significance GRCh37 chr12: 3,282,098-3,845,523 , GRCh38.p12 chr12: 3,172,932-3,736,357 CRACR2A, RPS26P44, 10 more genes
    nsv4674941copy number variation1nstd102humanPathogenic GRCh37 chr12: 274,676-37,869,301 , GRCh38.p12 chr12: 165,510-37,475,499 LOC105376675, ATF7IP, 682 more genes
    nsv4457052copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-6,346,092 , GRCh38.p12 chr12: 64,620-6,236,926 TSPAN9, RNU6-174P, 118 more genes
    nsv4455658copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-8,393,815 , GRCh38.p12 chr12: 64,620-8,241,219 PLEKHG6, MIR141, 226 more genes
    nsv4455458copy number variation1nstd102humanPathogenic GRCh37 chr12: 173,786-34,496,628 , GRCh38.p12 chr12: 64,620-34,343,693 EMP1, PLBD1-AS1, 684 more genes
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