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Items: 1 to 20 of 188

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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
    nsv7018029copy number variation1nstd229human GRCh38 chr19: 38,899,495-38,899,689 , GRCh37.p13 chr19: 39,390,135-39,390,329 SIRT2, NFKBIB
    nsv7015725copy number variation1nstd229human GRCh38 chr19: 38,859,787-38,882,916 , GRCh37.p13 chr19: 39,350,427-39,373,556 RINL, SIRT2
    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
    nsv6999783copy number variation1nstd229human GRCh38 chr19: 38,891,819-38,894,751 , GRCh37.p13 chr19: 39,382,459-39,385,391 SIRT2
    nsv6624467copy number variation2nstd224human GRCh37 chr19: 39,361,302-39,372,104 , GRCh38.p12 chr19: 38,870,662-38,881,464 , GRCh38.p12 chr19|NW_014040929.1: 280,334-291,136 SIRT2, RINL
    nsv6535366copy number variation1nstd223human GRCh38 chr19: 38,859,787-38,882,916 , GRCh37.p13 chr19: 39,350,427-39,373,556 SIRT2, RINL
    nsv6533394copy number variation1nstd223human GRCh38 chr19: 38,864,101-38,884,500 , GRCh37.p13 chr19: 39,354,741-39,375,140 SIRT2, RINL
    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
    nsv6531571copy number variation1nstd223human GRCh38 chr19: 38,884,607-38,887,096 , GRCh37.p13 chr19: 39,375,247-39,377,736 SIRT2
    nsv6526082copy number variation1nstd223human GRCh38 chr19: 38,885,647-38,886,678 , GRCh37.p13 chr19: 39,376,287-39,377,318 SIRT2
    nsv6524996copy number variation1nstd223human GRCh38 chr19: 38,897,789-38,898,814 , GRCh37.p13 chr19: 39,388,429-39,389,454 NFKBIB, SIRT2
    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
    nsv6145831copy number variation1nstd206human GRCh38 chr19: 38,896,874-38,904,874 , GRCh37.p13 chr19: 39,387,514-39,395,514 SIRT2, NFKBIB
    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
    nsv5927658copy number variation1nstd209human GRCh38 chr19: 38,876,987-38,877,576 , GRCh37.p13 chr19: 39,367,627-39,368,216 RINL, SIRT2
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