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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967661insertion1nstd209human GRCh38 chr19: 35,511,510-35,511,510 , GRCh37.p13 chr19: 36,002,412-36,002,412 DMKN
    nsv5932460copy number variation1nstd209human GRCh38 chr19: 35,511,459-35,511,509 , GRCh37.p13 chr19: 36,002,361-36,002,411 DMKN
    nsv5703117mobile element insertion1nstd211human GRCh38 chr19: 35,500,171-35,500,171 , GRCh37.p13 chr19: 35,991,073-35,991,073 DMKN
    nsv5589253copy number variation1nstd207human GRCh38 chr19: 35,511,459-35,511,509 , GRCh37.p13 chr19: 36,002,361-36,002,411 DMKN
    nsv4907536mobile element deletion1nstd200human GRCh38 chr19: 35,496,382-35,496,679 , GRCh37.p13 chr19: 35,987,284-35,987,581 DMKN
    nsv4738219copy number variation1nstd199human GRCh37 chr19: 36,002,368-36,002,420 , GRCh38.p12 chr19: 35,511,466-35,511,518 DMKN
    nsv4724383insertion1nstd186human GRCh37 chr19: 36,002,412-36,002,412 , GRCh38.p12 chr19: 35,511,510-35,511,510 DMKN
    nsv4674329copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,553,425-36,264,299 , GRCh38.p12 chr19: 35,062,521-35,773,397 LOC105372379, LSR, 50 more genes
    nsv4545000insertion1nstd166human GRCh37.p13 chr19: 36,002,358-36,002,358 , GRCh38.p12 chr19: 35,511,456-35,511,456 DMKN
    nsv4541179insertion1nstd166human GRCh37.p13 chr19: 36,002,412-36,002,412 , GRCh38.p12 chr19: 35,511,510-35,511,510 DMKN
    nsv4457800copy number variation1nstd102humanUncertain significance GRCh37 chr19: 35,613,953-36,183,886 , GRCh38.p12 chr19: 35,123,049-35,692,984 SBSN, UPK1A, 38 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
    nsv4414303copy number variation1nstd174human GRCh37 chr19: 36,002,361-36,002,431 , GRCh38.p12 chr19: 35,511,459-35,511,529 DMKN
    nsv4350190copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,043,556-36,316,644 , GRCh38.p12 chr19: 34,552,651-35,825,742 SCN1B, ETV2, 76 more genes
    nsv4349605copy number variation1nstd102humanPathogenic GRCh37 chr19: 35,111,811-37,744,992 , GRCh38.p12 chr19: 34,620,906-37,254,090 ATP4A, RNY5P10, 129 more genes
    nsv4271087copy number variation1nstd166human GRCh37.p13 chr19: 36,002,358-36,002,422 , GRCh38.p12 chr19: 35,511,456-35,511,520 DMKN
    nsv4269926copy number variation1nstd166human GRCh37.p13 chr19: 36,002,403-36,002,470 , GRCh38.p12 chr19: 35,511,501-35,511,568 DMKN
    nsv4263987copy number variation1nstd166human GRCh37.p13 chr19: 35,987,284-35,987,581 , GRCh38.p12 chr19: 35,496,382-35,496,679 DMKN
    nsv4259840copy number variation1nstd166human GRCh37.p13 chr19: 35,995,776-36,009,032 , GRCh38.p12 chr19: 35,504,874-35,518,130 DMKN
    nsv4254162copy number variation1nstd166human GRCh37.p13 chr19: 35,986,481-35,990,780 , GRCh38.p12 chr19: 35,495,579-35,499,878 DMKN
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