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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3914018copy number variation1nstd102humanLikely benign NCBI36 chr15: 63,025,681-63,085,686 , GRCh37 chr15: 65,238,628-65,298,633 , GRCh38 chr15: 64,946,408-65,006,295 SPG21, MTFMT, 1 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 SPG21, H3P40, 1616 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 SPG21, RNU6-18P, 1442 more genes
    nsv3900281copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,016,811-102,493,540 , GRCh38.p12 chr15: 19,811,558-101,953,337 SPG21, MYZAP, 1750 more genes
    nsv3913581copy number variation1nstd102humanPathogenic NCBI36 chr15: 18,323,354-100,338,915 , GRCh37.p13 chr15: 20,063,340-102,521,392 , GRCh38.p12 chr15: 19,858,087-101,981,189 SPG21, MIR4513, 1754 more genes
    nsv3904086copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,071,673-102,461,162 , GRCh38.p12 chr15: 19,866,420-101,920,959 SPG21, TMEM202, 1747 more genes
    nsv3905138copy number variation1nstd102humanPathogenic GRCh37 chr15: 20,733,395-102,511,616 , GRCh38.p12 chr15: 20,528,156-101,971,413 SPG21, FES, 1738 more genes
    nsv3892955copy number variation2nstd102humanPathogenic GRCh37 chr15: 22,770,422-102,429,112 , GRCh38.p12 chr15: 23,319,714-101,888,909 SPG21, FAM81A, 1614 more genes
    nsv3876912copy number variation1nstd102humanPathogenic GRCh37 chr15: 31,115,047-102,354,857 , GRCh38.p12 chr15: 30,822,844-101,814,654 SPG21, RNU6-953P, 1385 more genes
    nsv3899559copy number variation1nstd102humanPathogenic GRCh37 chr15: 41,745,084-102,354,798 , GRCh38.p12 chr15: 41,452,886-101,814,595 SPG21, CILP, 1176 more genes
    nsv3917589copy number variation1nstd102humanPathogenic GRCh37 chr15: 60,120,659-102,461,201 , GRCh38 chr15: 59,828,460-101,920,998 , NCBI36 chr15: 57,907,951-100,278,724 SPG21, GAPDHP61, 840 more genes
    nsv3895615copy number variation1nstd102humanPathogenic GRCh37 chr15: 64,637,227-102,509,910 , GRCh38.p12 chr15: 64,345,028-101,969,707 SPG21, KRT18P47, 781 more genes
    nsv3912545copy number variation1nstd102humanPathogenic GRCh37 chr15: 64,741,035-66,267,777 , GRCh38 chr15: 64,448,836-65,975,439 , NCBI36 chr15: 62,528,088-64,054,831 SPG21, LOC105370861, 44 more genes
    nsv3883273copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 63,414,894-66,439,797 , GRCh38.p12 chr15: 63,122,695-66,147,459 SPG21, CA12, 66 more genes
    nsv3905308copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 59,297,293-102,480,888 , GRCh38.p12 chr15: 59,005,094-101,940,685 SPG21, ACAN, 861 more genes
    nsv4729728copy number variation1nstd102humanUncertain significance GRCh37 chr15: 65,221,723-65,365,642 , GRCh38.p12 chr15: 64,929,524-65,073,304 SPG21, RASL12, 4 more genes
    nsv6309801copy number variation1nstd102humanUncertain significance GRCh37 chr15: 65,255,951-65,370,540 , GRCh38.p12 chr15: 64,963,610-65,078,202 SPG21, MTFMT, 4 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 SPG21, SNRPCP18, 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 SPG21, SNORD116-23, 1622 more genes
    nsv3909919copy number variation1nstd102humanUncertain significance GRCh38 chr15: 64,671,902-65,034,346 , NCBI36 chr15: 62,751,154-63,113,737 , GRCh37 chr15: 64,964,101-65,326,684 SPG21, PLEKHO2, 8 more genes
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