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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7068813inversion1nstd229human GRCh38 chr19: 56,872,783-57,542,535 , GRCh37.p13 chr19: 57,384,151-58,053,903 ZNF550, ZNF773, 25 more genes
    nsv6999110copy number variation1nstd229human GRCh38 chr19: 57,288,372-57,890,926 , GRCh37.p13 chr19: 57,799,740-58,402,294 ZNF460, ZNF551, 32 more genes
    nsv6625051copy number variation1nstd224human GRCh37 chr19: 56,901,396-57,956,715 , GRCh38.p12 chr19: 56,390,027-57,445,347 AURKC, ZIM2, 42 more genes
    nsv6597711inversion1nstd223human GRCh38 chr19: 55,930,883-58,410,519 , GRCh37.p13 chr19: 56,442,249-58,921,886 ZNF667-AS1, ZNF606-AS1, 130 more genes
    nsv6597167inversion1nstd223human GRCh38 chr19: 55,930,699-58,410,630 , GRCh37.p13 chr19: 56,442,065-58,921,997 VN2R19P, RPL19P19, 130 more genes
    nsv6133477copy number variation1nstd213human GRCh37 chr19: 57,800,000-59,128,983 , GRCh38.p12 chr19: 57,288,632-58,607,616 A1BG, FKBP1AP1, 95 more genes
    nsv6133413copy number variation1nstd213human GRCh37 chr19: 57,870,000-59,128,983 , GRCh38.p12 chr19: 57,358,632-58,607,616 ZNF8, ZNF211, 92 more genes
    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
    nsv5206770mobile element deletion1nstd204human GRCh37.p13 chr19: 57,877,180-57,877,508 , GRCh38.p13 chr19: 57,365,812-57,366,140 ZNF547, TRAPPC2B
    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
    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 LOC107987270, MIR6799, 694 more genes
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