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Items: 1 to 20 of 165

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5027885copy number variation1nstd200human GRCh38 chr19: 38,634,505-38,640,202 , GRCh37.p13 chr19: 39,125,145-39,130,842 EIF3K
    nsv5027884copy number variation1nstd200human GRCh38 chr19: 38,633,345-38,639,145 , GRCh37.p13 chr19: 39,123,985-39,129,785 EIF3K
    nsv5027883copy number variation1nstd200human GRCh38 chr19: 38,628,738-38,633,600 , GRCh37.p13 chr19: 39,119,378-39,124,240 EIF3K
    nsv5027882copy number variation1nstd200human GRCh38 chr19: 38,625,449-38,627,608 , GRCh37.p13 chr19: 39,116,089-39,118,248 EIF3K
    nsv5024619copy number variation1nstd200human GRCh38 chr19: 38,634,428-38,647,163 , GRCh37.p13 chr19: 39,125,068-39,137,803 ACTN4, EIF3K
    nsv4868295copy number variation1nstd200human GRCh37 chr19: 39,123,985-39,129,785 , GRCh38.p12 chr19: 38,633,345-38,639,145 , GRCh38.p12 chr19|NW_014040929.1: 42,981-48,781 EIF3K
    nsv4676223copy number variation1nstd102humanUncertain significance GRCh37 chr19: 38,512,717-39,291,526 , GRCh38.p12 chr19: 38,022,077-38,800,886 MAP4K1-AS1, LGALS7B, 25 more genes
    nsv4634245copy number variation1nstd183human GRCh37 chr19: 39,097,677-39,174,332 , GRCh38.p12 chr19|NW_014040929.1: 16,673-93,328 , GRCh38.p12 chr19: 38,607,037-38,683,692 ACTN4, EIF3K, 1 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4262470copy number variation1nstd166human GRCh37.p13 chr19: 39,121,596-39,142,654 , GRCh38.p12 chr19|NW_014040929.1: 40,592-61,650 , GRCh38.p12 chr19: 38,630,956-38,652,014 ACTN4, EIF3K
    nsv4258957copy number variation1nstd166human GRCh37.p13 chr19: 39,120,865-39,120,915 , GRCh38.p12 chr19|NW_014040929.1: 39,861-39,911 , GRCh38.p12 chr19: 38,630,225-38,630,275 EIF3K
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