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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3906801copy number variation1nstd102humanBenign GRCh37 chr16: 3,705,015-3,721,773 , GRCh38.p12 chr16: 3,655,014-3,671,772 DNASE1, TRAP1
    nsv3892824copy number variation1nstd102humanBenign GRCh37 chr16: 3,705,015-3,718,848 , GRCh38.p12 chr16: 3,655,014-3,668,847 DNASE1, TRAP1
    nsv3922524copy number variation1nstd102humanLikely benign NCBI36 chr16: 3,644,630-3,656,084 , GRCh38 chr16: 3,654,628-3,666,082 , GRCh37 chr16: 3,704,629-3,716,083 DNASE1, TRAP1
    nsv3911054copy number variation1nstd102humanLikely benign GRCh37 chr16: 3,707,044-3,716,083 , NCBI36 chr16: 3,647,045-3,656,084 , GRCh38 chr16: 3,657,043-3,666,082 DNASE1, TRAP1
    nsv6637609copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,695,926-3,764,880 , GRCh38.p12 chr16: 3,645,925-3,714,879 DNASE1, TRAP1
    nsv4455121copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,701,564-3,728,099 , GRCh38.p12 chr16: 3,651,563-3,678,098 DNASE1, TRAP1
    nsv3894218copy number variation2nstd102humanUncertain significance GRCh37 chr16: 3,701,564-3,726,595 , GRCh38.p12 chr16: 3,651,563-3,676,594 DNASE1, TRAP1
    nsv6637637copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,701,565-3,726,595 , GRCh38.p12 chr16: 3,651,564-3,676,594 DNASE1, TRAP1
    nsv4456529copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,694,758-3,716,657 , GRCh38.p12 chr16: 3,644,757-3,666,656 DNASE1, TRAP1
    nsv4455109copy number variation5nstd102humanUncertain significance GRCh37 chr16: 3,701,564-3,717,022 , GRCh38.p12 chr16: 3,651,563-3,667,021 DNASE1, TRAP1
    nsv3898143copy number variation1nstd102humanconflicting data from submitters GRCh37 chr16: 3,704,963-3,716,018 , GRCh38.p12 chr16: 3,654,962-3,666,017 DNASE1, TRAP1
    nsv6309907copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,705,375-3,716,139 , GRCh38.p12 chr16: 3,655,374-3,666,138 DNASE1, TRAP1
    nsv3909969copy number variation1nstd102humanPathogenic NCBI36 chr16: 3,597,089-3,867,322 , GRCh37 chr16: 3,657,088-3,927,321 , GRCh38 chr16: 3,607,087-3,877,320 DNASE1, TRAP1, 2 more genes
    nsv3903815copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,649,387-3,800,697 , GRCh38.p12 chr16: 3,599,386-3,750,696 DNASE1, SLX4, 2 more genes
    nsv6309865copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,711,968-3,781,958 , GRCh38.p12 chr16: 3,661,967-3,731,957 DNASE1, TRAP1, 1 more genes
    nsv3902056copy number variation1nstd102humanLikely benign GRCh37 chr16: 3,631,189-3,726,595 , GRCh38.p12 chr16: 3,581,188-3,676,594 DNASE1, SLX4, 2 more genes
    nsv3912877copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,900,735-7,160,698 , NCBI36 chr16: 2,840,736-7,100,699 , GRCh38 chr16: 2,850,734-7,110,697 DNASE1, TRP-CGG1-2, 129 more genes
    nsv3909798copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,146,027-6,362,229 , GRCh38.p12 chr16: 3,096,026-6,312,228 DNASE1, LINC01569, 102 more genes
    nsv6314863copy number variation1nstd102humanPathogenic GRCh38 chr16: 3,619,617-4,448,281 , GRCh37.p13 chr16: 3,669,618-4,498,282 DNASE1, TRAP1, 15 more genes
    nsv3917367copy number variation1nstd102humanPathogenic GRCh38 chr16: 3,560,564-4,266,796 , GRCh37 chr16: 3,610,565-4,316,797 , NCBI36 chr16: 3,550,566-4,256,798 DNASE1, TRAP1, 11 more genes
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