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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094391copy number variation1nstd102humanPathogenic GRCh37 chr15: 56,961,021-57,839,688 , GRCh38.p12 chr15: 56,668,823-57,547,490 ZNF280D, LOC107984759, 11 more genes
    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
    nsv6961650copy number variation1nstd229human GRCh38 chr15: 56,842,601-56,866,700 , GRCh37.p13 chr15: 57,134,799-57,158,898 LOC645877
    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
    nsv6507887copy number variation1nstd223human GRCh38 chr15: 56,838,307-56,921,338 , GRCh37.p13 chr15: 57,130,505-57,213,536 TCF12, LINC03065, 2 more genes
    nsv6502999copy number variation1nstd223human GRCh38 chr15: 56,798,325-56,860,901 , GRCh37.p13 chr15: 57,090,523-57,153,099 LOC645877
    nsv6291481copy number variation1nstd102humanPathogenic GRCh37 chr15: 55,772,371-57,880,518 , GRCh38.p12 chr15: 55,480,173-57,588,320 PRTG, LOC390586, 27 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
    nsv5939599copy number variation1nstd209human GRCh38 chr15: 56,780,964-56,943,658 , GRCh37.p13 chr15: 57,073,162-57,235,856 LOC645877, LINC03065, 2 more genes
    nsv5863202copy number variation1nstd209human GRCh38 chr15: 56,844,114-56,848,143 , GRCh37.p13 chr15: 57,136,312-57,140,341 LOC645877
    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
    nsv5005451copy number variation1nstd200human GRCh38 chr15: 56,838,307-56,921,339 , GRCh37.p13 chr15: 57,130,505-57,213,537 LOC645877, TCF12, 2 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
    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
    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
    nsv3919468copy number variation1nstd102humanPathogenic NCBI36 chr15: 26,996,912-100,338,915 , GRCh37.p13 chr15: 29,209,620-102,521,392 , GRCh38.p12 chr15: 28,917,417-101,981,189 RNU6-18P, GOLGA8K, 1442 more genes
    nsv3918770copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,280,728-100,338,915 , GRCh37.p13 chr15: 22,729,364-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNRPCP18, SNORD116-30, 1622 more genes
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