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Items: 1 to 20 of 218

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077519inversion1nstd229human GRCh38 chr12: 86,495,718-92,133,299 , GRCh37.p13 chr12: 86,889,495-92,527,075 CEP290, MIR3059, 60 more genes
    nsv7070941inversion1nstd229human GRCh38 chr12: 90,998,357-90,999,487 , GRCh37.p13 chr12: 91,392,134-91,393,264 EPYC
    nsv7067352inversion1nstd229human GRCh38 chr12: 90,985,236-90,987,355 , GRCh37.p13 chr12: 91,379,013-91,381,132 EPYC
    nsv7067281inversion1nstd229human GRCh38 chr12: 91,001,259-91,017,639 , GRCh37.p13 chr12: 91,395,036-91,411,416 EPYC
    nsv7060010inversion1nstd229human GRCh38 chr12: 86,085,575-91,207,469 , GRCh37.p13 chr12: 86,479,353-91,601,246 POC1B, C12orf50, 55 more genes
    nsv6936209copy number variation1nstd229human GRCh38 chr12: 90,992,531-91,003,199 , GRCh37.p13 chr12: 91,386,308-91,396,976 EPYC
    nsv6934679copy number variation1nstd229human GRCh38 chr12: 90,974,160-91,138,037 , GRCh37.p13 chr12: 91,367,937-91,531,814 KERA, EPYC, 1 more genes
    nsv6931050copy number variation1nstd229human GRCh38 chr12: 90,958,590-90,963,911 , GRCh37.p13 chr12: 91,352,367-91,357,688 EPYC
    nsv6930208copy number variation1nstd229human GRCh38 chr12: 90,978,343-91,040,984 , GRCh37.p13 chr12: 91,372,120-91,434,761 EPYC
    nsv6928187copy number variation1nstd229human GRCh38 chr12: 90,990,544-91,018,290 , GRCh37.p13 chr12: 91,384,321-91,412,067 EPYC
    nsv6927695copy number variation1nstd229human GRCh38 chr12: 90,167,236-91,253,354 , GRCh37.p13 chr12: 90,561,013-91,647,131 LOC105369895, EPYC, 8 more genes
    nsv6922173copy number variation1nstd229human GRCh38 chr12: 90,850,701-91,231,900 , GRCh37.p13 chr12: 91,244,478-91,625,677 LINC00615, CCER1, 4 more genes
    nsv6635205copy number variation1nstd227human GRCh38.p12 chr12: 90,940,828-91,012,761 , GRCh37 chr12: 91,334,605-91,406,538 EPYC, CCER1, 1 more genes
    nsv6621898copy number variation1nstd224human GRCh37 chr12: 91,363,838-91,380,633 , GRCh38.p12 chr12: 90,970,061-90,986,856 EPYC
    nsv6621897copy number variation1nstd224human GRCh37 chr12: 90,560,078-91,630,155 , GRCh38.p12 chr12: 90,166,301-91,236,378 LINC00615, LINC02822, 8 more genes
    nsv6621758copy number variation1nstd224human GRCh37 chr12: 90,562,017-91,630,155 , GRCh38.p12 chr12: 90,168,240-91,236,378 DCN, EPYC, 8 more genes
    nsv6588400inversion1nstd223human GRCh38 chr12: 90,985,240-90,987,355 , GRCh37.p13 chr12: 91,379,017-91,381,132 EPYC
    nsv6473381copy number variation1nstd223human GRCh38 chr12: 91,001,101-91,001,619 , GRCh37.p13 chr12: 91,394,878-91,395,396 EPYC
    nsv6473233copy number variation1nstd223human GRCh38 chr12: 90,983,156-90,983,583 , GRCh37.p13 chr12: 91,376,933-91,377,360 EPYC
    nsv6473226copy number variation1nstd223human GRCh38 chr12: 90,940,516-91,014,093 , GRCh37.p13 chr12: 91,334,293-91,407,870 EPYC, CCER1, 1 more genes
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