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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071327inversion1nstd229human GRCh38 chr15: 55,806,321-63,352,065 , GRCh37.p13 chr15: 56,098,519-63,644,264 LOC107984805, TPM1-AS, 120 more genes
    nsv7069841inversion1nstd229human GRCh38 chr15: 55,108,583-62,405,114 , GRCh37.p13 chr15: 55,400,781-62,697,313 LOC105370834, RPL21P14, 118 more genes
    nsv6963338copy number variation1nstd229human GRCh38 chr15: 57,717,901-57,729,400 , GRCh37.p13 chr15: 58,010,099-58,021,598 GCOM1, POLR2M
    nsv6959734copy number variation1nstd229human GRCh38 chr15: 57,704,445-57,705,070 , GRCh37.p13 chr15: 57,996,643-57,997,268 GCOM1, POLR2M
    nsv6959286copy number variation1nstd229human GRCh38 chr15: 57,704,575-57,705,071 , GRCh37.p13 chr15: 57,996,773-57,997,269 GCOM1, POLR2M
    nsv6637384copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,589,845-63,543,438 , GRCh38.p12 chr15: 48,297,648-63,251,239 LINC03065, FAM227B, 228 more genes
    nsv6513179copy number variation1nstd223human GRCh38 chr15: 54,191,007-57,968,497 , GRCh37.p13 chr15: 54,483,204-58,260,695 HMGB1P33, LOC105370829, 43 more genes
    nsv6133149copy number variation1nstd213human GRCh37 chr15: 57,070,000-59,480,001 , GRCh38.p12 chr15: 56,777,802-59,187,802 ADAM10, LIPC, 42 more genes
    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
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
    nsv4863827copy number variation1nstd200human GRCh37 chr15: 57,674,517-58,754,690 , GRCh38.p12 chr15: 57,382,319-58,462,491 , MTND6P23, 16 more genes
    nsv4729247copy number variation1nstd102humanUncertain significance GRCh37 chr15: 57,414,627-58,960,510 , GRCh38.p12 chr15: 57,122,429-58,668,311 RPL28P4, SNORD13D, 22 more genes
    nsv4680670copy number variation1nstd189human GRCh37.p13 chr15: 57,838,940-58,072,720 , GRCh38.p12 chr15: 57,546,742-57,780,522 POLR2M, CGNL1, 4 more genes
    nsv4675497copy number variation1nstd102humanLikely benign GRCh37 chr15: 57,350,251-58,025,960 , GRCh38.p12 chr15: 57,058,053-57,733,762 NDUFB10P1, LOC105370834, 12 more genes
    nsv4625290copy number variation1nstd183human GRCh37 chr15: 57,350,965-58,070,807 , GRCh38.p12 chr15: 57,058,767-57,778,609 NDUFB10P1, LOC105370834, 12 more genes
    nsv4456196copy number variation1nstd102humanPathogenic GRCh37 chr15: 48,000,433-60,747,551 , GRCh38.p12 chr15: 47,708,236-60,455,352 MIR1266, AQP9, 199 more genes
    nsv4368274copy number variation1nstd173human GRCh37 chr15: 57,859,275-59,410,122 , GRCh38.p12 chr15: 57,567,077-59,117,923 , RPL28P4, 28 more genes
    nsv3922157copy number variation1nstd102humanUncertain significance NCBI36 chr15: 29,852,369-100,338,915 , GRCh37.p13 chr15: 32,065,077-102,521,392 , GRCh38.p12 chr15: 31,772,874-101,981,189 GCHFR, SPPL2A, 1382 more genes
    nsv3921425copy number variation1nstd102humanPathogenic NCBI36 chr15: 55,647,440-61,098,667 , GRCh37 chr15: 57,860,148-63,311,614 , GRCh38 chr15: 57,567,950-63,019,415 MESTP2, HMGB1P51, 86 more genes
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