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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145272insertion1nstd232human GRCh37.p13 chr19: 39,111,077-39,111,077 , GRCh38.p12 chr19: 38,620,437-38,620,437 , GRCh38.p12 chr19|NW_014040929.1: 30,073-30,073 EIF3K
    nsv7095479copy number variation1nstd102humanUncertain significance GRCh37 chr19: 38,375,572-39,738,787 , GRCh38.p12 chr19: 37,884,932-39,248,147 HNRNPL, RN7SL663P, 45 more genes
    nsv7012392copy number variation1nstd229human GRCh38 chr19: 38,628,901-38,633,500 , GRCh37.p13 chr19: 39,119,541-39,124,140 EIF3K
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv6534030copy number variation1nstd223human GRCh38 chr19: 38,634,478-38,647,051 , GRCh37.p13 chr19: 39,125,118-39,137,691 EIF3K, ACTN4
    nsv6529745copy number variation1nstd223human GRCh38 chr19: 38,620,843-38,641,584 , GRCh37.p13 chr19: 39,111,483-39,132,224 EIF3K
    nsv6521669copy number variation1nstd223human GRCh38 chr19: 38,634,507-38,640,200 , GRCh37.p13 chr19: 39,125,147-39,130,840 EIF3K
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6223314copy number variation1nstd214human GRCh38 chr19: 38,630,224-38,630,274 , GRCh37.p13 chr19: 39,120,864-39,120,914 EIF3K
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv5975812insertion1nstd209human GRCh38 chr19: 38,637,325-38,637,325 , GRCh37.p13 chr19: 39,127,965-39,127,965 EIF3K
    nsv5945032copy number variation1nstd209human GRCh38 chr19: 38,630,224-38,630,274 , GRCh37.p13 chr19: 39,120,864-39,120,914 EIF3K
    nsv5937672copy number variation1nstd209human GRCh38 chr19: 38,548,476-38,693,241 , GRCh37.p13 chr19: 39,039,116-39,183,881 ACTN4, RYR1, 3 more genes
    nsv5526873copy number variation1nstd206human GRCh38 chr19: 38,628,403-38,628,790 , GRCh37.p13 chr19: 39,119,043-39,119,430 EIF3K
    nsv5524828copy number variation1nstd206human GRCh38 chr19: 38,630,225-38,630,275 , GRCh37.p13 chr19: 39,120,865-39,120,915 EIF3K
    nsv5517130copy number variation1nstd206human GRCh38 chr19: 38,634,432-38,643,913 , GRCh37.p13 chr19: 39,125,072-39,134,553 EIF3K
    nsv5329382copy number variation1nstd204human GRCh38.p13 chr19: 38,633,340-38,639,154 , GRCh37.p13 chr19: 39,123,980-39,129,794 EIF3K
    nsv5321553copy number variation1nstd204human GRCh38.p13 chr19: 38,630,216-38,630,283 , GRCh37.p13 chr19: 39,120,856-39,120,923 EIF3K
    nsv5289271copy number variation1nstd204human GRCh38.p13 chr19: 38,633,288-38,644,231 , GRCh37.p13 chr19: 39,123,928-39,134,871 EIF3K
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