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Items: 1 to 20 of 289

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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
    nsv7069328inversion1nstd229human GRCh38 chr19: 38,959,890-38,966,023 , GRCh37.p13 chr19: 39,450,530-39,456,663 FBXO17
    nsv7014270copy number variation1nstd229human GRCh38 chr19: 38,937,101-38,943,000 , GRCh37.p13 chr19: 39,427,741-39,433,640 FBXO17
    nsv7011903copy number variation1nstd229human GRCh38 chr19: 38,948,101-38,952,100 , GRCh37.p13 chr19: 39,438,741-39,442,740 FBXO17
    nsv7011727copy number variation1nstd229human GRCh38 chr19: 38,952,157-38,954,824 , GRCh37.p13 chr19: 39,442,797-39,445,464 FBXO17
    nsv7011596copy number variation1nstd229human GRCh38 chr19: 38,968,101-38,970,900 , GRCh37.p13 chr19: 39,458,741-39,461,540 FBXO17
    nsv7011539copy number variation1nstd229human GRCh38 chr19: 38,962,901-38,967,764 , GRCh37.p13 chr19: 39,453,541-39,458,404 FBXO17
    nsv7008190copy number variation1nstd229human GRCh38 chr19: 38,948,208-38,960,741 , GRCh37.p13 chr19: 39,438,848-39,451,381 FBXO17
    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
    nsv7008082copy number variation1nstd229human GRCh38 chr19: 38,949,480-38,984,502 , GRCh37.p13 chr19: 39,440,120-39,475,142 FBXO17
    nsv7005806copy number variation1nstd229human GRCh38 chr19: 38,963,001-38,967,800 , GRCh37.p13 chr19: 39,453,641-39,458,440 FBXO17
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv7004928copy number variation1nstd229human GRCh38 chr19: 38,941,110-38,944,511 , GRCh37.p13 chr19: 39,431,750-39,435,151 FBXO17
    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
    nsv6598983inversion1nstd223human GRCh38 chr19: 38,959,889-38,966,028 , GRCh37.p13 chr19: 39,450,529-39,456,668 FBXO17
    nsv6595716inversion1nstd223human GRCh38 chr19: 38,972,348-38,972,948 , GRCh37.p13 chr19: 39,462,988-39,463,588 FBXO17
    nsv6533968copy number variation1nstd223human GRCh38 chr19: 38,943,326-38,960,819 , GRCh37.p13 chr19: 39,433,966-39,451,459 FBXO17
    nsv6532144copy number variation1nstd223human GRCh38 chr19: 38,949,144-38,957,489 , GRCh37.p13 chr19: 39,439,784-39,448,129 FBXO17
    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
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