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Items: 1 to 20 of 324

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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
    nsv7009534copy number variation1nstd229human GRCh38 chr19: 1,090,366-1,108,431 , GRCh37.p13 chr19: 1,090,365-1,108,430 POLR2E, SBNO2, 1 more genes
    nsv7007680copy number variation1nstd229human GRCh38 chr19: 1,077,202-1,085,468 , GRCh37.p13 chr19: 1,077,201-1,085,467 POLR2E, ARHGAP45
    nsv6597832inversion1nstd223human GRCh38 chr19: 558,351-1,188,654 , GRCh37.p13 chr19: 558,351-1,188,653 HCN2, TMEM259, 40 more genes
    nsv6517008copy number variation1nstd223human GRCh38 chr19: 1,090,626-1,097,345 , GRCh37.p13 chr19: 1,090,625-1,097,344 POLR2E
    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
    nsv6307527copy number variation1nstd186human GRCh37 chr19: 1,033,799-1,267,999 , GRCh38.p12 chr19: 1,033,800-1,268,000 CIRBP, LOC102723811, 16 more genes
    nsv6289060insertion1nstd214human GRCh38 chr19: 1,085,864-1,085,864 , GRCh37.p13 chr19: 1,085,863-1,085,863 ARHGAP45, POLR2E
    nsv6189800copy number variation1nstd214human GRCh38 chr19: 1,085,483-1,085,584 , GRCh37.p13 chr19: 1,085,482-1,085,583 POLR2E, ARHGAP45
    nsv6145724copy number variation1nstd206human GRCh38 chr19: 1,033,800-1,268,000 , GRCh37.p13 chr19: 1,033,799-1,267,999 GPX4, CIRBP, 16 more genes
    nsv6133707copy number variation1nstd213human GRCh37 chr19: 560,000-1,700,001 , GRCh38.p12 chr19: 560,000-1,700,002 ATP5F1D, AZU1, 73 more genes
    nsv6133692copy number variation1nstd213human GRCh37 chr19: 180,000-2,200,001 , GRCh38.p12 chr19: 180,000-2,200,002 ATP5F1D, AZU1, 113 more genes
    nsv6102682inversion1nstd212human GRCh38 chr19: 871,904-2,377,665 , GRCh37.p13 chr19: 871,904-2,377,663 AMH, ATP5F1D, 83 more genes
    nsv6056050copy number variation1nstd212human GRCh38 chr19: 1,092,306-1,092,431 , GRCh37.p13 chr19: 1,092,305-1,092,430 POLR2E
    nsv6050337copy number variation1nstd212human GRCh38 chr19: 1,085,501-1,085,604 , GRCh37.p13 chr19: 1,085,500-1,085,603 ARHGAP45, POLR2E
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