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Items: 1 to 20 of 332

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3890948copy number variation1nstd102humanBenign GRCh37 chr16: 15,489,920-15,567,615 , GRCh38.p12 chr16: 15,396,063-15,473,758 , GRCh38.p12 chr16|NT_187607.1: 1,054,026-1,131,755 BMERB1, MPV17L
    nsv3901162copy number variation1nstd102humanBenign GRCh37 chr16: 15,469,950-15,661,789 , GRCh38.p12 chr16: 15,376,093-15,567,932 , GRCh38.p12 chr16|NT_187607.1: 1,034,042-1,225,924 BMERB1, MPV17L, 2 more genes
    nsv6291517copy number variation1nstd102humanLikely benign GRCh37 chr16: 15,481,920-15,617,999 , GRCh38.p12 chr16: 15,388,063-15,524,142 , GRCh38.p12 chr16|NT_187607.1: 1,046,027-1,182,135 BMERB1, MPV17L, 1 more genes
    nsv4675885copy number variation1nstd102humanUncertain significance GRCh37 chr16: 15,481,920-15,628,438 , GRCh38.p12 chr16|NT_187607.1: 1,046,027-1,192,573 , GRCh38.p12 chr16: 15,388,063-15,534,581 BMERB1, MPV17L, 1 more genes
    nsv4681164copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,680,574-15,932,109 , GRCh38.p12 chr16: 15,586,717-15,838,252 , GRCh38.p12 chr16|NT_187607.1: 1,244,709-1,496,241 BMERB1, MYH11, 4 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 BMERB1, 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 BMERB1, MIR6511A1, 82 more genes
    nsv3904576copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,318,664-18,778,064 , GRCh38.p12 chr16: 15,224,807-18,766,742 BMERB1, 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 BMERB1, 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 BMERB1, 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 BMERB1, 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 BMERB1, 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 BMERB1, 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 BMERB1, RNU6-213P, 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 BMERB1, TCERG1P2, 37 more genes
    nsv3914781copy number variation1nstd102humanPathogenic NCBI36 chr16: 15,458,563-18,214,342 , GRCh37 chr16: 15,551,062-18,306,841 , GRCh38 chr16: 15,457,205-18,212,984 BMERB1, RPL7P47, 36 more genes
    nsv3895083copy number variation1nstd102humanPathogenic GRCh37 chr16: 15,481,920-18,181,971 , GRCh38.p12 chr16|NT_187607.1: 1,046,027-2,659,700 , GRCh38.p12 chr16: 15,388,063-18,088,114 BMERB1, MIR6770-2, 35 more genes
    nsv3924171copy number variation1nstd102humanPathogenic NCBI36 chr16: 15,399,808-18,069,668 , GRCh38 chr16: 15,398,450-18,068,310 , GRCh37 chr16: 15,492,307-18,162,167 BMERB1, LOC105371100, 35 more genes
    nsv3898601copy number variation3nstd102humannot provided, Pathogenic GRCh37 chr16: 15,494,600-18,141,051 , GRCh38.p12 chr16: 15,400,743-18,047,194 , GRCh38.p12 chr16|NT_187607.1: 1,058,708-2,659,700 BMERB1, LOC105371099, 35 more genes
    nsv3917876copy number variation2nstd102humanUncertain significance, Pathogenic GRCh38 chr16: 15,434,653-18,055,828 , GRCh37 chr16: 15,528,510-18,149,685 , NCBI36 chr16: 15,436,011-18,057,186 BMERB1, ABCC1, 34 more genes
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