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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5380762copy number variation1nstd102humanUncertain significance GRCh37 chr15: 44,855,319-45,898,712 , GRCh38.p12 chr15: 44,563,121-45,606,514 LOC100533853, RNU6-1108P, 44 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
    nsv5005337copy number variation1nstd200human GRCh38 chr15: 44,757,662-45,480,882 , GRCh37.p13 chr15: 45,049,860-45,773,080 DUOXA1, TRH-GTG1-7, 34 more genes
    nsv5005336copy number variation1nstd200human GRCh38 chr15: 44,757,739-45,467,369 , GRCh37.p13 chr15: 45,049,937-45,759,567 TRH-GTG1-9, LOC100533853, 33 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
    nsv4729351copy number variation1nstd102humanUncertain significance GRCh37 chr15: 45,056,077-45,772,378 , GRCh38.p12 chr15: 44,763,879-45,480,180 LOC100187725, DUOXA2, 34 more genes
    nsv4683408copy number variation1nstd102humanUncertain significance GRCh37 chr15: 45,654,287-45,670,671 , GRCh38.p12 chr15: 45,362,089-45,378,473 GATM
    nsv4633164copy number variation1nstd183human GRCh37 chr15: 45,049,695-45,772,448 , GRCh38.p12 chr15: 44,757,497-45,480,250 TRH-GTG1-9, TRH-GTG1-8, 34 more genes
    nsv4629775copy number variation1nstd183human GRCh37 chr15: 45,643,203-45,653,950 , GRCh38.p12 chr15: 45,351,005-45,361,752 RNU6-953P, GATM
    nsv4622619copy number variation1nstd183human GRCh37 chr15: 45,050,604-45,769,052 , GRCh38.p12 chr15: 44,758,406-45,476,854 LOC100129830, SLC30A4-AS1, 33 more genes
    nsv4456158copy number variation1nstd102humanUncertain significance GRCh37 chr15: 45,063,803-45,772,378 , GRCh38.p12 chr15: 44,771,605-45,480,180 TRH-GTG1-9, DUOX2, 33 more genes
    nsv4245771copy number variation1nstd166human GRCh37.p13 chr15: 45,674,301-45,675,920 , GRCh38.p12 chr15: 45,382,103-45,383,722 GATM
    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
    nsv3922111copy number variation1nstd102humanUncertain significance NCBI36 chr15: 42,826,429-43,583,911 , GRCh37.p13 chr15: 45,039,137-45,796,619 , GRCh38.p12 chr15: 44,746,939-45,504,421 H3P39, DUOX2, 34 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
    nsv3918644copy number variation1nstd102humanUncertain significance NCBI36 chr15: 20,313,935-100,338,915 , GRCh37.p13 chr15: 22,762,571-102,521,392 , GRCh38.p12 chr15: 23,319,714-101,981,189 SNORD116-23, UBE2Q2P6, 1622 more genes
    nsv3916249copy number variation1nstd102humanPathogenic NCBI36 chr15: 21,173,967-100,338,915 , GRCh37.p13 chr15: 23,622,526-102,521,392 , GRCh38.p12 chr15: 23,377,379-101,981,189 H3P40, EEF1B2P1, 1616 more genes
    nsv3915618copy number variation1nstd102humanUncertain significance NCBI36 chr15: 42,845,404-43,556,344 , GRCh37 chr15: 45,058,112-45,769,052 , GRCh38 chr15: 44,765,914-45,476,854 RNU1-119P, SORD, 33 more genes
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