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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095297copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-5,696,788 , GRCh38.p12 chr19: 589,946-5,696,777 NCLN, RN7SL202P, 223 more genes
    nsv7095296copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-2,151,333 , GRCh38.p12 chr19: 589,946-2,151,334 ADAMTSL5, GPX4, 90 more genes
    nsv7095226copy number variation1nstd102humanUncertain significance GRCh37 chr19: 589,946-4,818,389 , GRCh38.p12 chr19: 589,946-4,818,377 ATP5F1D, LOC102723798, 204 more genes
    nsv7073159inversion1nstd229human GRCh38 chr19: 249,047-1,189,238 , GRCh37.p13 chr19: 249,047-1,189,237 MADCAM1-AS1, ARID3A, 53 more genes
    nsv7064913inversion1nstd229human GRCh38 chr19: 558,352-1,188,612 , GRCh37.p13 chr19: 558,352-1,188,611 MIR4745, R3HDM4, 40 more genes
    nsv7058460inversion1nstd229human GRCh38 chr19: 322,195-777,239 , GRCh37.p13 chr19: 322,195-777,239 PRSS57, RPS2P52, 23 more genes
    nsv7016597copy number variation1nstd229human GRCh38 chr19: 606,901-620,700 , GRCh37.p13 chr19: 606,901-620,700 POLRMT, HCN2, 1 more genes
    nsv7014719copy number variation1nstd229human GRCh38 chr19: 633,395-633,531 , GRCh37.p13 chr19: 633,395-633,531 LOC105372234, POLRMT
    nsv7014503copy number variation1nstd229human GRCh38 chr19: 622,109-633,960 , GRCh37.p13 chr19: 622,109-633,960 LOC105372234, POLRMT
    nsv7013390copy number variation1nstd229human GRCh38 chr19: 588,683-616,954 , GRCh37.p13 chr19: 588,683-616,954 HCN2, POLRMT, 2 more genes
    nsv7006552copy number variation1nstd229human GRCh38 chr19: 629,485-631,577 , GRCh37.p13 chr19: 629,485-631,577 POLRMT
    nsv7005970copy number variation1nstd229human GRCh38 chr19: 617,704-621,768 , GRCh37.p13 chr19: 617,704-621,768 POLRMT
    nsv7001195copy number variation1nstd229human GRCh38 chr19: 632,079-676,330 , GRCh37.p13 chr19: 632,079-676,330 POLRMT, RNF126, 3 more genes
    nsv7000456copy number variation1nstd229human GRCh38 chr19: 599,363-727,471 , GRCh37.p13 chr19: 599,363-727,471 PRSS57, POLRMT, 8 more genes
    nsv6597832inversion1nstd223human GRCh38 chr19: 558,351-1,188,654 , GRCh37.p13 chr19: 558,351-1,188,653 HCN2, TMEM259, 40 more genes
    nsv6521993copy number variation1nstd223human GRCh38 chr19: 606,158-635,412 , GRCh37.p13 chr19: 606,158-635,412 LOC107987266, HCN2, 2 more genes
    nsv6519957copy number variation1nstd223human GRCh38 chr19: 630,987-635,717 , GRCh37.p13 chr19: 630,987-635,717 LOC105372234, POLRMT
    nsv6315518copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-2,256,387 , GRCh38.p12 chr19: 260,911-2,256,388 LOC100420586, RPS15, 113 more genes
    nsv6315510copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-1,319,319 , GRCh38.p12 chr19: 260,911-1,319,320 LOC101928450, LOC105372235, 66 more genes
    nsv6205139copy number variation1nstd214human GRCh38 chr19: 632,045-632,125 , GRCh37.p13 chr19: 632,045-632,125 LOC105372234, POLRMT
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