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Items: 1 to 20 of 22

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 TSEN34, ZNF321P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 TSEN34, BABAM1, 2426 more genes
    nsv3903092copy number variation2nstd102humanPathogenic GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521 TSEN34, LENG8, 2408 more genes
    nsv3919076copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,432,832-59,083,573 , NCBI36 chr19: 53,124,644-63,775,385 , GRCh38 chr19: 47,929,575-58,572,206 TSEN34, KCNA7, 697 more genes
    nsv3911950copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,411,797-59,051,332 , NCBI36 chr19: 53,103,609-63,743,144 , GRCh38 chr19: 47,908,540-58,539,965 TSEN34, LOC107987270, 694 more genes
    nsv3924732copy number variation1nstd102humanPathogenic GRCh38 chr19: 49,907,832-58,557,889 , GRCh37 chr19: 50,411,089-59,069,256 , NCBI36 chr19: 55,102,901-63,761,068 TSEN34, RPL39P37, 556 more genes
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 TSEN34, SIGLEC5, 574 more genes
    nsv3890862copy number variation1nstd102humanPathogenic GRCh37 chr19: 50,489,390-59,095,359 , GRCh38.p12 chr19: 49,986,133-58,583,992 TSEN34, SIGLECL1, 552 more genes
    nsv3923909copy number variation1nstd102humanPathogenic NCBI36 chr19: 55,347,589-63,784,382 , GRCh37 chr19: 50,655,777-59,092,570 , GRCh38 chr19: 50,152,520-58,581,203 TSEN34, OSCAR, 535 more genes
    nsv3891963copy number variation1nstd102humanPathogenic GRCh37 chr19: 50,740,074-59,097,160 , GRCh38.p12 chr19: 50,236,817-58,585,793 TSEN34, RPS9, 535 more genes
    nsv3916611copy number variation1nstd102humanPathogenic GRCh37 chr19: 50,694,476-59,047,185 , NCBI36 chr19: 55,386,288-63,738,997 , GRCh38 chr19: 50,191,219-58,535,818 TSEN34, RNU6-980P, 526 more genes
    nsv3922599copy number variation1nstd102humanPathogenic GRCh38 chr19: 51,141,518-58,539,965 , NCBI36 chr19: 56,336,587-63,743,144 , GRCh37 chr19: 51,644,775-59,051,332 TSEN34, LOC100421130, 475 more genes
    nsv3913991copy number variation1nstd102humanPathogenic NCBI36 chr19: 57,338,938-63,648,700 , GRCh37 chr19: 52,647,126-58,956,888 , GRCh38 chr19: 52,143,873-58,445,521 TSEN34, PEG3, 398 more genes
    nsv3923613copy number variation1nstd102humanPathogenic GRCh38 chr19: 52,612,432-58,581,203 , GRCh37 chr19: 53,115,685-59,092,570 , NCBI36 chr19: 57,807,497-63,784,382 TSEN34, ZNF71-SMIM17, 393 more genes
    nsv3919766copy number variation1nstd102humanPathogenic NCBI36 chr19: 58,150,121-63,784,382 , GRCh37 chr19: 53,458,309-59,092,570 , GRCh38 chr19: 52,955,056-58,581,203 TSEN34, MIR520F, 382 more genes
    nsv3890688copy number variation1nstd102humanPathogenic GRCh37 chr19: 54,196,216-58,759,679 , GRCh38.p12 chr19: 53,692,962-58,248,313 TSEN34, MIR517C, 283 more genes
    nsv1398372copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,647,215-54,705,417 , GRCh38.p12 chr19: 54,143,479-54,201,549 , GRCh38.p12 chr19|NW_003571057.2: 118,328-176,531 , GRCh38.p12 chr19|NW_003571056.2: 118,328-176,531 , GRCh38.p12 chr19|NW_003571055.2: 134,805-176,531 , GRCh38.p12 chr19|NW_003571054.1: 118,328-176,348 , GRCh38.p12 chr19|NT_187693.1: 134,805-176,531 , GRCh38.p12 chr19|NW_003571061.2: 118,328-176,531 , GRCh38.p12 chr19|NW_003571059.2: 118,328-176,531 , GRCh38.p12 chr19|NW_003571058.2: 118,328-176,531 , GRCh38.p12 chr19|NW_003571060.1: 118,328-176,521 TSEN34, MBOAT7, 5 more genes
    nsv4730034copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,334,195-56,434,037 , GRCh38.p12 chr19: 53,830,941-55,922,671 , GRCh38.p12 chr19|NT_187693.1: 1-1,066,800 , GRCh38.p12 chr19|NW_003571057.2: 1-1,091,841 , GRCh38.p12 chr19|NW_003571058.2: 1-1,066,390 , GRCh38.p12 chr19|NW_003571056.2: 1-1,064,304 TSEN34, KIR3DP1, 133 more genes
    nsv3903661copy number variation1nstd102humanUncertain significance GRCh37 chr19: 53,867,570-55,833,460 , GRCh38.p12 chr19|NW_003571060.1: 1-987,100 , GRCh38.p12 chr19|NW_003571059.2: 1-1,002,683 , GRCh38.p12 chr19|NW_003571054.1: 1-987,716 , GRCh38.p12 chr19: 53,364,317-55,322,092 , GRCh38.p12 chr19|NW_003571058.2: 1-1,066,390 , GRCh38.p12 chr19|NT_187693.1: 1-1,066,800 , GRCh38.p12 chr19|NW_003571057.2: 1-1,091,841 , GRCh38.p12 chr19|NW_003571056.2: 1-1,064,304 TSEN34, MIR512-2, 180 more genes
    nsv6310493copy number variation1nstd102humanUncertain significance GRCh37 chr19: 54,297,303-55,678,016 , GRCh38.p12 chr19|NT_187693.1: 134,805-894,467 , GRCh38.p12 chr19: 53,794,049-55,166,648 TSEN34, PRPF31, 80 more genes
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