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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7095205copy number variation2nstd102humanUncertain significance GRCh37 chr19: 39,205,089-40,913,839 , GRCh38.p12 chr19: 38,714,449-40,407,932 CCNP, NFKBIB, 81 more genes
    nsv7064872inversion1nstd229human GRCh38 chr19: 38,901,471-38,917,132 , GRCh37.p13 chr19: 39,392,111-39,407,772 CCER2, NFKBIB, 1 more genes
    nsv7016591copy number variation1nstd229human GRCh38 chr19: 38,913,549-38,918,974 , GRCh37.p13 chr19: 39,404,189-39,409,614 SARS2, CCER2
    nsv7009986copy number variation1nstd229human GRCh38 chr19: 38,914,693-38,917,248 , GRCh37.p13 chr19: 39,405,333-39,407,888 SARS2, CCER2
    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
    nsv7002869copy number variation1nstd229human GRCh38 chr19: 38,872,385-39,331,882 , GRCh37.p13 chr19: 39,363,025-39,822,522 IFNL4P1, IFNL4, 19 more genes
    nsv6998425copy number variation1nstd229human GRCh38 chr19: 38,900,571-38,930,432 , GRCh37.p13 chr19: 39,391,211-39,421,072 NFKBIB, CCER2, 2 more genes
    nsv6531882copy number variation1nstd223human GRCh38 chr19: 38,872,385-39,331,882 , GRCh37.p13 chr19: 39,363,025-39,822,522 NFKBIB, IFNL3, 19 more genes
    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
    nsv6144358copy number variation1nstd206human GRCh38 chr19: 38,852,874-38,930,874 , GRCh37.p13 chr19: 39,343,514-39,421,514 NFKBIB, MRPS12, 4 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6109210insertion1nstd212human GRCh38 chr19: 38,920,705-38,920,705 , GRCh37.p13 chr19: 39,411,345-39,411,345 SARS2
    nsv6107991insertion1nstd212human GRCh38 chr19: 38,919,501-38,919,501 , GRCh37.p13 chr19: 39,410,141-39,410,141 SARS2
    nsv6102162insertion1nstd212human GRCh38 chr19: 38,920,764-38,920,764 , GRCh37.p13 chr19: 39,411,404-39,411,404 SARS2
    nsv5973074insertion1nstd209human GRCh38 chr19: 38,929,261-38,929,261 , GRCh37.p13 chr19: 39,419,901-39,419,901 SARS2, MRPS12
    nsv5931714copy number variation1nstd209human GRCh38 chr19: 38,916,801-38,917,100 , GRCh37.p13 chr19: 39,407,441-39,407,740 SARS2
    nsv5726633mobile element insertion2nstd211human GRCh38 chr19: 38,919,502-38,919,502 , GRCh37.p13 chr19: 39,410,142-39,410,142 SARS2
    nsv5561343mobile element insertion1nstd206human GRCh38 chr19: 38,919,502-38,919,553 , GRCh37.p13 chr19: 39,410,142-39,410,193 SARS2
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