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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077246inversion1nstd229human GRCh38 chr15: 64,487,767-67,498,498 , GRCh37.p13 chr15: 64,779,966-67,790,836 LETM1P1, MIR4512, 74 more genes
    nsv7069168inversion1nstd229human GRCh38 chr15: 65,085,774-67,006,275 , GRCh37.p13 chr15: 65,378,112-67,298,613 MEGF11, HNRNPA1P44, 51 more genes
    nsv7063733inversion1nstd229human GRCh38 chr15: 63,479,684-65,571,065 , GRCh37.p13 chr15: 63,771,883-65,863,403 TRIP4, RNU5B-1, 45 more genes
    nsv6975579copy number variation1nstd229human GRCh38 chr15: 65,132,701-65,145,200 , GRCh37.p13 chr15: 65,425,039-65,437,538 PDCD7
    nsv6964107copy number variation1nstd229human GRCh38 chr15: 65,127,219-65,132,129 , GRCh37.p13 chr15: 65,419,557-65,424,467 PDCD7
    nsv6960749copy number variation1nstd229human GRCh38 chr15: 65,122,991-65,124,915 , GRCh37.p13 chr15: 65,415,329-65,417,253 PDCD7
    nsv6959900copy number variation1nstd229human GRCh38 chr15: 65,121,766-65,137,055 , GRCh37.p13 chr15: 65,414,104-65,429,393 PDCD7
    nsv6584724inversion1nstd223human GRCh38 chr15: 65,122,791-65,123,428 , GRCh37.p13 chr15: 65,415,129-65,415,766 PDCD7
    nsv6314072copy number variation1nstd102humanUncertain significance GRCh37 chr15: 64,978,681-65,679,053 , GRCh38.p12 chr15: 64,686,482-65,386,715 CLPX, RNU5B-1, 22 more genes
    nsv6133150copy number variation1nstd213human GRCh37 chr15: 59,870,000-66,270,001 , GRCh38.p12 chr15: 59,577,801-65,977,663 GTF2A2, OAZ2, 115 more genes
    nsv5861109copy number variation1nstd209human GRCh38 chr15: 65,127,846-65,138,731 , GRCh37.p13 chr15: 65,420,184-65,431,069 PDCD7
    nsv5856850copy number variation1nstd209human GRCh38 chr15: 65,127,921-65,131,820 , GRCh37.p13 chr15: 65,420,259-65,424,158 PDCD7
    nsv5721720mobile element insertion2nstd211human GRCh38 chr15: 65,126,601-65,126,601 , GRCh37.p13 chr15: 65,418,939-65,418,939 PDCD7
    nsv5552192insertion1nstd206human GRCh38 chr15: 65,116,568-65,116,677 , GRCh37.p13 chr15: 65,408,906-65,409,015 PDCD7
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5197183mobile element insertion1nstd203human GRCh38 chr15: 65,126,595-65,126,601 , GRCh37.p13 chr15: 65,418,933-65,418,939 PDCD7
    nsv5188563mobile element insertion1nstd203human GRCh38 chr15: 65,126,590-65,126,601 , GRCh37.p13 chr15: 65,418,928-65,418,939 PDCD7
    nsv5155259mobile element insertion1nstd203human GRCh38 chr15: 65,116,635-65,116,677 , GRCh37.p13 chr15: 65,408,973-65,409,015 PDCD7
    nsv5142051mobile element insertion1nstd203human GRCh38 chr15: 65,127,419-65,127,434 , GRCh37.p13 chr15: 65,419,757-65,419,772 PDCD7
    nsv5005507copy number variation1nstd200human GRCh38 chr15: 65,122,991-65,124,915 , GRCh37.p13 chr15: 65,415,329-65,417,253 PDCD7
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