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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970408inversion1nstd209human GRCh38 chr19: 2,282,477-7,636,587 , GRCh37.p13 chr19: 2,282,476-7,701,473 , TLE5, 195 more genes
    nsv5942775copy number variation1nstd209human GRCh38 chr19: 2,865,023-7,153,898 , GRCh37.p13 chr19: 2,865,021-7,153,909 , GNA15-DT, 159 more genes
    nsv5932690copy number variation1nstd209human GRCh38 chr19: 4,308,728-4,308,854 , GRCh37.p13 chr19: 4,308,725-4,308,851 FSD1
    nsv5874110copy number variation1nstd209human GRCh38 chr19: 4,315,698-4,316,997 , GRCh37.p13 chr19: 4,315,695-4,316,994 FSD1
    nsv5662530insertion1nstd207human GRCh38 chr19: 4,321,225-4,321,225 , GRCh37.p13 chr19: 4,321,222-4,321,222 FSD1
    nsv5529659copy number variation1nstd206human GRCh38 chr19: 4,308,731-4,308,855 , GRCh37.p13 chr19: 4,308,728-4,308,852 FSD1
    nsv5514089copy number variation1nstd206human GRCh38 chr19: 4,320,829-4,321,225 , GRCh37.p13 chr19: 4,320,826-4,321,222 FSD1
    nsv5381793copy number variation1nstd102humanPathogenic GRCh37 chr19: 3,976,203-4,345,430 , GRCh38.p12 chr19: 3,976,205-4,345,433 MPND, SNORD37, 13 more genes
    nsv5292408copy number variation1nstd204human GRCh38.p13 chr19: 2,552,101-4,875,100 , GRCh37.p13 chr19: 2,552,099-4,875,112 , S1PR4, 93 more genes
    nsv5284500copy number variation1nstd204human GRCh38.p13 chr19: 4,068,001-4,541,200 , GRCh37.p13 chr19: 4,067,999-4,541,212 , EIF1P6, 20 more genes
    nsv5167881mobile element insertion1nstd203human GRCh38 chr19: 4,312,459-4,312,469 , GRCh37.p13 chr19: 4,312,456-4,312,466 FSD1
    nsv5027325copy number variation1nstd200human GRCh38 chr19: 4,319,864-4,320,449 , GRCh37.p13 chr19: 4,319,861-4,320,446 FSD1
    nsv5027324copy number variation1nstd200human GRCh38 chr19: 4,308,593-4,309,974 , GRCh37.p13 chr19: 4,308,590-4,309,971 FSD1
    nsv4852662copy number variation1nstd200human GRCh37 chr19: 4,320,583-4,321,100 , GRCh38.p12 chr19: 4,320,586-4,321,103 FSD1
    nsv4852661copy number variation1nstd200human GRCh37 chr19: 4,308,728-4,308,852 , GRCh38.p12 chr19: 4,308,731-4,308,855 FSD1
    nsv4852660copy number variation1nstd200human GRCh37 chr19: 4,302,644-4,303,259 , GRCh38.p12 chr19: 4,302,647-4,303,262 TMIGD2, FSD1
    nsv4765299insertion1nstd199human GRCh37 chr19: 4,321,219-4,321,219 , GRCh38.p12 chr19: 4,321,222-4,321,222 FSD1
    nsv4676189copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-4,384,674 , GRCh38.p12 chr19: 260,912-4,384,677 MRPL54, DAZAP1, 198 more genes
    nsv4629028copy number variation1nstd183human GRCh37 chr19: 4,310,337-4,310,543 , GRCh38.p12 chr19: 4,310,340-4,310,546 FSD1
    nsv4457776copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,911-4,788,357 , GRCh38.p12 chr19: 260,911-4,788,345 BSG, LOC100420586, 217 more genes
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