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Items: 1 to 20 of 98

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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
    nsv5028193copy number variation1nstd200human GRCh38 chr19: 57,420,167-57,421,184 , GRCh37.p13 chr19: 57,931,535-57,932,552 ZNF17
    nsv5028192copy number variation1nstd200human GRCh38 chr19: 57,409,264-57,411,113 , GRCh37.p13 chr19: 57,920,632-57,922,481 ZNF17
    nsv5025008copy number variation1nstd200human GRCh38 chr19: 57,412,483-57,419,129 , GRCh37.p13 chr19: 57,923,851-57,930,497 ZNF17
    nsv5025007copy number variation1nstd200human GRCh38 chr19: 57,409,336-57,411,104 , GRCh37.p13 chr19: 57,920,704-57,922,472 ZNF17
    nsv5025006copy number variation1nstd200human GRCh38 chr19: 57,404,109-57,438,820 , GRCh37.p13 chr19: 57,915,477-57,950,188 ZNF749, ZNF17
    nsv4865376copy number variation1nstd200human GRCh37 chr19: 57,923,852-57,930,497 , GRCh38.p12 chr19: 57,412,484-57,419,129 ZNF17
    nsv4865375copy number variation1nstd200human GRCh37 chr19: 57,915,477-57,950,188 , GRCh38.p12 chr19: 57,404,109-57,438,820 ZNF17, ZNF749
    nsv4715096translocation1nstd195human GRCh37 chr3: 169,602,027-169,602,027 , GRCh37 chr19: 57,925,696-57,925,696 , GRCh38.p12 chr19: 57,414,328-57,414,328 , GRCh38.p12 chr3: 169,884,239-169,884,239 ZNF17
    nsv4706698translocation1nstd195human GRCh37 chr3: 169,602,027-169,602,027 , GRCh37 chr19: 57,925,697-57,925,697 , GRCh38.p12 chr19: 57,414,329-57,414,329 , GRCh38.p12 chr3: 169,884,239-169,884,239 ZNF17
    nsv4575302mobile element insertion1nstd166human GRCh37.p13 chr19: 57,933,164-57,933,164 , GRCh38.p12 chr19: 57,421,796-57,421,796 ZNF17
    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
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