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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5938141copy number variation1nstd209human GRCh38 chr19: 58,188,253-58,189,852 , GRCh37.p13 chr19: 58,699,620-58,701,219 ZNF274
    nsv5933977copy number variation1nstd209human GRCh38 chr19: 58,212,389-58,212,454 , GRCh37.p13 chr19: 58,723,755-58,723,820 ZNF274
    nsv5929135copy number variation1nstd209human GRCh38 chr19: 58,184,858-58,185,165 , GRCh37.p13 chr19: 58,696,225-58,696,532 ZNF274
    nsv5869431copy number variation1nstd209human GRCh38 chr19: 58,188,583-58,190,203 , GRCh37.p13 chr19: 58,699,950-58,701,570 ZNF274
    nsv5280745copy number variation1nstd204human GRCh38.p13 chr19: 57,881,401-58,501,600 , GRCh37.p13 chr19: 58,392,769-59,012,967 ZNF417, LOC112268251, 51 more genes
    nsv5173649mobile element insertion1nstd203human GRCh38 chr19: 58,184,910-58,184,954 , GRCh37.p13 chr19: 58,696,277-58,696,321 ZNF274
    nsv5161454mobile element insertion1nstd203human GRCh38 chr19: 58,206,052-58,206,064 , GRCh37.p13 chr19: 58,717,419-58,717,431 ZNF274
    nsv5025025copy number variation1nstd200human GRCh38 chr19: 58,101,230-58,193,466 , GRCh37.p13 chr19: 58,612,597-58,704,833 ZSCAN18, ZNF329, 1 more genes
    nsv4865386copy number variation1nstd200human GRCh37 chr19: 58,612,597-58,704,833 , GRCh38.p12 chr19: 58,101,230-58,193,466 ZNF329, ZNF274, 1 more genes
    nsv4861535copy number variation1nstd200human GRCh37 chr19: 58,720,479-58,720,957 , GRCh38.p12 chr19: 58,209,113-58,209,591 ZNF274
    nsv4729813copy number variation1nstd102humanUncertain significance GRCh37 chr19: 58,687,912-58,946,147 , GRCh38.p12 chr19: 58,176,545-58,434,780 ZNF837, LOC100419840, 26 more genes
    nsv4676227copy number variation1nstd102humanUncertain significance GRCh37 chr19: 58,647,621-58,703,491 , GRCh38.p12 chr19: 58,136,254-58,192,124 ZNF329, ZNF274
    nsv4632108copy number variation1nstd183human GRCh37 chr19: 58,580,277-58,828,076 , GRCh38.p12 chr19: 58,068,909-58,316,710 ZNF329, ZSCAN18, 12 more genes
    nsv4544518insertion1nstd166human GRCh37.p13 chr19: 58,700,045-58,700,045 , GRCh38.p12 chr19: 58,188,678-58,188,678 ZNF274
    nsv4257075copy number variation1nstd166human GRCh37.p13 chr19: 58,720,479-58,720,957 , GRCh38.p12 chr19: 58,209,113-58,209,591 ZNF274
    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
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