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Items: 1 to 20 of 184

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071546inversion1nstd229human GRCh38 chr13: 52,130,547-52,541,062 , GRCh37.p13 chr13: 52,704,683-53,115,197 MRPS31P5, LOC101929657, 11 more genes
    nsv6952289copy number variation1nstd229human GRCh38 chr13: 46,982,261-52,142,641 , GRCh37.p13 chr13: 47,556,396-52,716,777 KCNRG, RNA5SP28, 99 more genes
    nsv6951969copy number variation1nstd229human GRCh38 chr13: 45,143,357-52,624,108 , GRCh37.p13 chr13: 45,717,492-53,198,243 SNRPGP14, EBPL, 158 more genes
    nsv6939912copy number variation1nstd229human GRCh38 chr13: 52,115,908-52,209,758 , GRCh37.p13 chr13: 52,690,044-52,783,893 NEK3, MRPS31P5, 3 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6622063copy number variation1nstd224human GRCh37 chr13: 52,679,373-52,792,819 , GRCh38.p12 chr13: 52,105,237-52,218,684 NEK3, NEK5, 4 more genes
    nsv6622062copy number variation1nstd224human GRCh37 chr13: 52,679,373-52,769,702 , GRCh38.p12 chr13: 52,105,237-52,195,567 NEK5, MRPS31P5, 3 more genes
    nsv6495186copy number variation1nstd223human GRCh38 chr13: 52,126,501-52,131,100 , GRCh37.p13 chr13: 52,700,637-52,705,236 NEK5, NEK3, 1 more genes
    nsv6490597copy number variation1nstd223human GRCh38 chr13: 52,115,908-52,209,726 , GRCh37.p13 chr13: 52,690,044-52,783,861 THSD1P1, NEK3, 3 more genes
    nsv6487902copy number variation1nstd223human GRCh38 chr13: 52,122,029-52,138,188 , GRCh37.p13 chr13: 52,696,165-52,712,324 NEK5, NEK3, 1 more genes
    nsv6315497copy number variation1nstd102humanUncertain significance GRCh37 chr13: 52,535,544-53,362,733 , GRCh38.p12 chr13: 51,961,408-52,788,598 HNRNPA1L2, NEK3, 19 more genes
    nsv6315495copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 RNU6-80P, EFNB2, 1334 more genes
    nsv6314198copy number variation1nstd102humanPathogenic GRCh37 chr13: 44,573,371-53,324,137 , GRCh38.p12 chr13: 43,999,235-52,750,002 PCNPP5, NRAD1, 189 more genes
    nsv6314117copy number variation1nstd102humanPathogenic GRCh37 chr13: 36,376,204-80,681,753 , GRCh38.p12 chr13: 35,802,067-80,107,618 RBM26, RNY4P31, 591 more genes
    nsv6314030copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,436,286-114,981,726 , GRCh38.p12 chr13: 18,862,146-114,216,251 RPSAP53, LOC105370213, 1310 more genes
    nsv6291487copy number variation1nstd102humanPathogenic GRCh37 chr13: 42,504,540-108,206,269 , GRCh38.p12 chr13: 41,930,404-107,553,921 CALM2P4, RNU6-81P, 778 more genes
    nsv6290319copy number variation1nstd102humanPathogenic GRCh37 chr13: 45,819,046-63,910,212 , GRCh38.p12 chr13: 45,244,911-63,336,079 CNMD, CPB2-AS1, 241 more genes
    nsv6289999copy number variation1nstd102humanPathogenic GRCh37 chr13: 1-115,169,878 , GRCh38.p12 chr13: 18,445,862-114,344,403 LINC00363, LOC105370118, 1334 more genes
    nsv6249070mobile element insertion1nstd215human GRCh38 chr13: 52,129,749-52,129,749 , GRCh37.p13 chr13: 52,703,885-52,703,885 LOC101929657
    nsv6133100copy number variation1nstd213human GRCh37 chr13: 52,550,000-56,590,001 , GRCh38.p12 chr13: 51,975,864-56,015,867 ATP7B, NEK3, 34 more genes
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