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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5380841copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr15: 72,978,549-73,029,948 , GRCh38.p12 chr15: 72,686,208-72,737,607 HIGD2B, BBS4
    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
    nsv5009051copy number variation1nstd200human GRCh38 chr15: 72,677,383-72,677,740 , GRCh37.p13 chr15: 72,969,724-72,970,081 HIGD2B
    nsv4992279copy number variation1nstd200human GRCh38 chr15: 72,675,079-72,677,884 , GRCh37.p13 chr15: 72,967,420-72,970,225 HIGD2B
    nsv4992278copy number variation1nstd200human GRCh38 chr15: 72,673,181-72,677,873 , GRCh37.p13 chr15: 72,965,522-72,970,214 HIGD2B
    nsv4728893copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 70,268,937-74,098,081 , GRCh38.p12 chr15: 69,976,598-73,805,740 BBS4, FKBP1AP2, 75 more genes
    nsv4683941copy number variation1nstd102humanUncertain significance GRCh37 chr15: 72,646,022-73,660,621 , GRCh38.p12 chr15: 72,353,681-73,368,280 TMEM202, PHB1P20, 24 more genes
    nsv4682188copy number variation1nstd102humanUncertain significance GRCh37 chr15: 72,968,375-72,996,856 , GRCh38.p12 chr15: 72,676,034-72,704,515 BBS4, HIGD2B
    nsv4573331mobile element insertion1nstd166human GRCh37.p13 chr15: 72,976,449-72,976,449 , GRCh38.p12 chr15: 72,684,108-72,684,108 HIGD2B
    nsv4530572copy number variation1nstd166human GRCh37.p13 chr15: 72,969,724-72,970,081 , GRCh38.p12 chr15: 72,677,383-72,677,740 HIGD2B
    nsv4529101copy number variation1nstd166human GRCh37.p13 chr15: 72,959,999-73,050,000 , GRCh38.p12 chr15: 72,667,658-72,757,659 HIGD2B, GOLGA6B, 2 more genes
    nsv4456455copy number variation1nstd102humanUncertain significance GRCh37 chr15: 72,825,914-73,067,234 , GRCh38.p12 chr15: 72,533,573-72,774,893 ARIH1, MIR630, 9 more genes
    nsv4455940copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,943,184-75,544,524 , GRCh38.p12 chr15: 72,650,843-75,252,183 TBC1D21, CPLX3, 72 more genes
    nsv4455912copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,963,271-76,064,900 , GRCh38.p12 chr15: 72,670,930-75,772,559 MIR6881, ARID3B, 94 more genes
    nsv4455687copy number variation1nstd102humanPathogenic GRCh37 chr15: 72,926,922-75,544,524 , GRCh38.p12 chr15: 72,634,581-75,252,183 SCAMP2, LOC105376731, 74 more genes
    nsv4376076copy number variation1nstd173human GRCh37 chr15: 72,930,208-72,971,911 , GRCh38.p12 chr15: 72,637,867-72,679,570 GOLGA6B, RN7SL853P, 2 more genes
    nsv4243342copy number variation1nstd166human GRCh37.p13 chr15: 72,962,000-72,967,100 , GRCh38.p12 chr15: 72,669,659-72,674,759 HIGD2B
    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
    nsv3920789copy number variation1nstd102humanLikely pathogenic NCBI36 chr15: 70,751,023-73,279,197 , GRCh37 chr15: 72,963,970-75,492,144 , GRCh38 chr15: 72,671,629-75,199,803 BBS4, CLK3, 67 more genes
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