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Items: 1 to 20 of 94

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5292903copy number variation1nstd204human GRCh38.p13 chr19: 57,172,601-57,751,900 , GRCh37.p13 chr19: 57,683,969-58,263,268 TPRG1LP1, ZNF805, 30 more genes
    nsv5280624copy number variation1nstd204human GRCh38.p13 chr19: 57,527,801-57,913,300 , GRCh37.p13 chr19: 58,039,169-58,424,668 ZNF549, ZNF417, 19 more genes
    nsv5025013copy number variation1nstd200human GRCh38 chr19: 57,662,149-57,967,273 , GRCh37.p13 chr19: 58,173,517-58,478,641 ZNF814, C19orf18, 16 more genes
    nsv4631981copy number variation1nstd183human GRCh37 chr19: 58,167,451-58,210,489 , GRCh38.p12 chr19: 57,656,083-57,699,121 ZNF154, ZNF551, 2 more genes
    nsv4506926mobile element insertion1nstd166human GRCh37.p13 chr19: 58,174,710-58,174,710 , GRCh38.p12 chr19: 57,663,342-57,663,342 TPRG1LP1, ZSCAN4
    nsv4457732copy number variation1nstd102humanUncertain significance GRCh37 chr19: 57,952,073-58,661,581 , GRCh38.p12 chr19: 57,440,705-58,150,214 ZNF418, ZNF606-AS1, 39 more genes
    nsv4457626copy number variation1nstd102humanUncertain significance GRCh37 chr19: 58,092,045-58,686,148 , GRCh38.p12 chr19: 57,580,677-58,174,781 ZNF417, ZSCAN1, 30 more genes
    nsv4457535copy number variation1nstd102humanUncertain significance GRCh37 chr19: 58,054,819-58,410,552 , GRCh38.p12 chr19: 57,543,451-57,899,184 ZNF587B, ZNF530, 17 more genes
    nsv4257508copy number variation1nstd166human GRCh37.p13 chr19: 58,173,517-58,478,693 , GRCh38.p12 chr19: 57,662,149-57,967,325 C19orf18, ZNF586, 16 more genes
    nsv3924817copy number variation1nstd102humanUncertain significance GRCh37 chr19: 58,057,811-58,401,314 , NCBI36 chr19: 62,749,623-63,093,126 , GRCh38 chr19: 57,546,443-57,889,946 ZNF211, FKBP1AP1, 17 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 RPL39P37, CCDC106, 556 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 OSCAR, FKBP1AP1, 535 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 ZNF71-SMIM17, MIR518E, 393 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 LOC100421130, A1BG-AS1, 475 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 MIR520F, A1BG-AS1, 382 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 KCNA7, ZNF28, 697 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 RNU6-980P, ERVV-1, 526 more genes
    nsv3916295copy number variation1nstd102humanPathogenic NCBI36 chr19: 61,566,389-63,784,382 , GRCh37 chr19: 56,874,577-59,092,570 , GRCh38 chr19: 56,363,208-58,581,203 ZIM2, LOC100419848, 131 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 PEG3, ZNF480, 398 more genes
    nsv3912907copy number variation1nstd102humanUncertain significance GRCh38 chr19: 56,353,449-58,445,521 , NCBI36 chr19: 61,556,630-63,648,700 , GRCh37 chr19: 56,864,818-58,956,888 MIR4754, ZNF460-AS1, 114 more genes
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