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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7005446copy number variation1nstd229human GRCh38 chr19: 29,661,628-29,664,861 , GRCh37.p13 chr19: 30,152,535-30,155,768 LOC105372353, PLEKHF1
    nsv6527526copy number variation1nstd223human GRCh38 chr19: 28,925,173-32,768,942 , GRCh37.p13 chr19: 29,416,080-33,259,848 DPY19L3, CCNE1, 50 more genes
    nsv6526233copy number variation1nstd223human GRCh38 chr19: 28,377,231-29,769,380 , GRCh37.p13 chr19: 28,868,138-30,260,287 LINC01532, C19orf12, 16 more genes
    nsv6518001copy number variation1nstd223human GRCh38 chr19: 29,670,225-29,676,531 , GRCh37.p13 chr19: 30,161,132-30,167,438 PLEKHF1
    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
    nsv5024519copy number variation1nstd200human GRCh38 chr19: 28,925,173-32,768,971 , GRCh37.p13 chr19: 29,416,080-33,259,877 , LOC105372355, 53 more genes
    nsv5020231copy number variation1nstd200human GRCh38 chr19: 29,671,393-29,675,925 , GRCh37.p13 chr19: 30,162,300-30,166,832 PLEKHF1
    nsv5020230copy number variation1nstd200human GRCh38 chr19: 29,670,210-29,676,522 , GRCh37.p13 chr19: 30,161,117-30,167,429 PLEKHF1
    nsv5020164copy number variation1nstd200human GRCh38 chr19: 28,377,231-29,769,380 , GRCh37.p13 chr19: 28,868,138-30,260,287 , LINC00906, 18 more genes
    nsv4861162copy number variation1nstd200human GRCh37 chr19: 30,162,300-30,166,832 , GRCh38.p12 chr19: 29,671,393-29,675,925 PLEKHF1
    nsv4729940copy number variation1nstd102humanUncertain significance GRCh37 chr19: 29,739,728-31,053,524 , GRCh38.p12 chr19: 29,248,821-30,562,617 PLEKHF1, RPL9P32, 12 more genes
    nsv4702925copy number variation1nstd195human GRCh38.p12 chr19: 29,514,544-29,719,294 , GRCh37 chr19: 30,005,451-30,210,201 POP4, PLEKHF1, 4 more genes
    nsv4630420copy number variation1nstd183human GRCh37 chr19: 27,749,407-30,499,419 , GRCh38.p12 chr19: 27,258,499-30,008,512 , C19orf12, 32 more genes
    nsv4623792copy number variation1nstd183human GRCh37 chr19: 30,159,691-30,256,478 , GRCh38.p12 chr19: 29,668,784-29,765,571 LOC107985345, PLEKHF1, 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
    nsv4269222copy number variation1nstd166human GRCh37.p13 chr19: 30,147,455-30,167,458 , GRCh38.p12 chr19: 29,656,548-29,676,551 PLEKHF1, LOC105372353
    nsv3920776copy number variation1nstd102humanLikely pathogenic NCBI36 chr19: 34,234,635-37,150,342 , GRCh37 chr19: 29,542,795-32,458,502 , GRCh38 chr19: 29,051,888-31,967,596 CCNE1, UQCRFS1, 30 more genes
    nsv3919618copy number variation1nstd102humanUncertain significance NCBI36 chr19: 32,962,986-39,966,686 , GRCh38 chr19: 27,780,238-34,783,942 , GRCh37 chr19: 28,271,146-35,274,846 LINC00906, TDRD12, 112 more genes
    nsv3919296copy number variation1nstd102humanPathogenic NCBI36 chr19: 34,844,605-43,297,203 , GRCh37 chr19: 30,152,765-38,605,363 , GRCh38 chr19: 29,661,858-38,114,723 UBA2, ZNF529, 241 more genes
    nsv3916007copy number variation1nstd102humanPathogenic GRCh37 chr19: 30,162,231-38,393,630 , NCBI36 chr19: 34,854,071-43,085,470 , GRCh38 chr19: 29,671,324-37,902,990 MAG, RNU6-967P, 238 more genes
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