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Items: 1 to 20 of 341

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3905535copy number variation1nstd102humanBenign GRCh37 chr16: 16,071,849-16,077,360 , GRCh38.p12 chr16: 15,977,992-15,983,503 , GRCh38.p12 chr16|NT_187607.1: 1,635,970-1,641,481 ABCC1
    nsv3910227copy number variation1nstd102humanLikely benign NCBI36 chr16: 15,939,156-15,956,160 , GRCh37 chr16: 16,031,655-16,048,659 , GRCh38 chr16: 15,937,798-15,954,802 ABCC1, LOC107984869
    nsv4675252copy number variation1nstd102humanPathogenic GRCh37 chr16: 16,099,145-16,295,901 , GRCh38.p12 chr16: 16,005,288-16,202,044 , GRCh38.p12 chr16|NT_187607.1: 1,663,167-1,860,042 ABCC1, ABCC6, 1 more genes
    nsv4729760copy number variation1nstd102humanLikely benign GRCh37 chr16: 16,146,794-16,293,305 , GRCh38.p12 chr16: 16,052,937-16,199,448 , GRCh38.p12 chr16|NT_187607.1: 1,710,835-1,857,446 ABCC1, RPL17P40, 1 more genes
    nsv3913131copy number variation1nstd102humanBenign GRCh37 chr16: 15,986,060-16,041,539 , NCBI36 chr16: 15,893,561-15,949,040 , GRCh38 chr16: 15,892,203-15,947,682 ABCC1, LOC107984869, 1 more genes
    nsv4675985copy number variation1nstd102humanUncertain significance GRCh37 chr16: 16,052,972-16,330,627 , GRCh38.p12 chr16: 15,959,115-16,236,770 , GRCh38.p12 chr16|NT_187607.1: 1,617,093-1,894,768 ABCC1, LOC105371100, 3 more genes
    nsv3901756copy number variation1nstd102humanUncertain significance GRCh37 chr16: 16,060,396-16,294,705 , GRCh38.p12 chr16: 15,966,539-16,200,848 , GRCh38.p12 chr16|NT_187607.1: 1,624,517-1,858,846 ABCC1, ABCC6, 1 more genes
    nsv3923795copy number variation1nstd102humanUncertain significance NCBI36 chr16: 16,050,797-16,189,886 , GRCh37.p13 chr16: 16,143,296-16,282,385 , GRCh38.p12 chr16: 16,049,439-16,188,528 , GRCh38.p12 chr16|NT_187607.1: 1,707,336-1,846,531 ABCC1, RPL17P40, 1 more genes
    nsv3915661copy number variation1nstd102humanUncertain significance NCBI36 chr16: 16,120,173-16,235,416 , GRCh37.p13 chr16: 16,212,672-16,327,915 , GRCh38.p12 chr16: 16,118,815-16,234,058 , GRCh38.p12 chr16|NT_187607.1: 1,776,680-1,892,056 ABCC1, LOC105371100, 2 more genes
    nsv3885195copy number variation1nstd102humanPathogenic GRCh38 chr16: 15,788,690-16,185,034 , GRCh37.p13 chr16: 15,882,547-16,278,891 ABCC1, ABCC6, 6 more genes
    nsv3916649copy number variation1nstd102humanPathogenic NCBI36 chr16: 14,760,627-18,687,298 , GRCh37.p13 chr16: 14,853,126-18,779,797 , GRCh38.p12 chr16: 14,759,269-18,768,475 , GRCh38.p12 chr16|NT_187607.1: 293,011-2,659,700 ABCC1, RRN3, 90 more genes
    nsv3920316copy number variation1nstd102humanPathogenic GRCh38 chr16: 14,816,348-18,658,403 , NCBI36 chr16: 14,817,706-18,577,226 , GRCh37 chr16: 14,910,205-18,669,725 ABCC1, MIR6511A1, 82 more genes
    nsv3904576copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,318,664-18,778,064 , GRCh38.p12 chr16: 15,224,807-18,766,742 ABCC1, RPL7P47, 58 more genes
    nsv3923793copy number variation1nstd102humanPathogenic NCBI36 chr16: 15,141,934-18,577,226 , GRCh37 chr16: 15,234,433-18,669,725 , GRCh38 chr16: 15,140,576-18,658,403 ABCC1, LOC102723692, 62 more genes
    nsv3921429copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,917,806-18,149,685 , GRCh38 chr16: 14,823,949-18,055,828 , NCBI36 chr16: 14,825,307-18,057,186 ABCC1, NOMO1, 61 more genes
    nsv3922278copy number variation1nstd102humanPathogenic GRCh37 chr16: 14,910,205-18,141,051 , GRCh38 chr16: 14,816,348-18,047,194 , NCBI36 chr16: 14,817,706-18,048,552 ABCC1, MIR6770-1, 61 more genes
    nsv3904490copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,316,618-18,181,971 , GRCh38.p12 chr16: 15,222,761-18,088,114 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-2,659,700 ABCC1, NDE1, 37 more genes
    nsv7148112copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,489,453-18,321,582 , GRCh38.p12 chr16: 15,395,596-18,227,725 , GRCh38.p12 chr16|NT_187607.1: 1,053,559-2,659,700 ABCC1, MIR484, 37 more genes
    nsv4729445copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,375,911-18,198,455 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-2,659,700 , GRCh38.p12 chr16: 15,282,054-18,104,598 ABCC1, BMERB1, 38 more genes
    nsv4674979copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,416,364-18,231,275 , GRCh38.p12 chr16|NT_187607.1: 1,015,619-2,659,700 , GRCh38.p12 chr16: 15,322,507-18,137,418 ABCC1, TCERG1P2, 37 more genes
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