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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977986insertion1nstd209human GRCh38 chr15: 50,216,611-50,216,611 , GRCh37.p13 chr15: 50,508,808-50,508,808 SLC27A2
    nsv5973387insertion1nstd209human GRCh38 chr15: 50,196,078-50,196,078 , GRCh37.p13 chr15: 50,488,275-50,488,275 SLC27A2
    nsv5946069copy number variation1nstd209human GRCh38 chr15: 50,202,918-50,204,202 , GRCh37.p13 chr15: 50,495,115-50,496,399 SLC27A2
    nsv5710054mobile element insertion1nstd211human GRCh38 chr15: 50,196,078-50,196,078 , GRCh37.p13 chr15: 50,488,275-50,488,275 SLC27A2
    nsv5662953insertion1nstd207human GRCh38 chr15: 50,229,239-50,229,239 , GRCh37.p13 chr15: 50,521,436-50,521,436 SLC27A2
    nsv5647843insertion1nstd207human GRCh38 chr15: 50,206,149-50,206,149 , GRCh37.p13 chr15: 50,498,346-50,498,346 SLC27A2
    nsv5531231copy number variation1nstd206human GRCh38 chr15: 50,202,029-50,202,102 , GRCh37.p13 chr15: 50,494,226-50,494,299 SLC27A2
    nsv5523535copy number variation1nstd206human GRCh38 chr15: 50,229,239-50,229,540 , GRCh37.p13 chr15: 50,521,436-50,521,737 SLC27A2
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5314349copy number variation1nstd204human GRCh38.p13 chr15: 50,229,215-50,229,569 , GRCh37.p13 chr15: 50,521,412-50,521,766 SLC27A2
    nsv5191606mobile element insertion1nstd203human GRCh38 chr15: 50,196,476-50,196,490 , GRCh37.p13 chr15: 50,488,673-50,488,687 SLC27A2
    nsv5149381mobile element insertion1nstd203human GRCh38 chr15: 50,233,744-50,233,755 , GRCh37.p13 chr15: 50,525,941-50,525,952 SLC27A2
    nsv5147574mobile element insertion1nstd203human GRCh38 chr15: 50,196,053-50,196,078 , GRCh37.p13 chr15: 50,488,250-50,488,275 SLC27A2
    nsv5143618mobile element insertion1nstd203human GRCh38 chr15: 50,196,060-50,196,078 , GRCh37.p13 chr15: 50,488,257-50,488,275 SLC27A2
    nsv5143097mobile element insertion1nstd203human GRCh38 chr15: 50,196,075-50,196,097 , GRCh37.p13 chr15: 50,488,272-50,488,294 SLC27A2
    nsv5038422inversion1nstd200human GRCh38 chr15: 40,121,948-64,050,807 , GRCh37.p13 chr15: 40,414,149-64,343,006 , EIF4EBP2P2, 475 more genes
    nsv5007518copy number variation1nstd200human GRCh38 chr15: 50,228,863-50,230,021 , GRCh37.p13 chr15: 50,521,060-50,522,218 SLC27A2
    nsv5007517copy number variation1nstd200human GRCh38 chr15: 50,202,943-50,204,203 , GRCh37.p13 chr15: 50,495,140-50,496,400 SLC27A2
    nsv5005382copy number variation1nstd200human GRCh38 chr15: 50,229,239-50,229,540 , GRCh37.p13 chr15: 50,521,436-50,521,737 SLC27A2
    nsv4872280inversion1nstd200human GRCh37 chr15: 40,414,149-64,343,008 , GRCh38.p12 chr15: 40,121,948-64,050,809 , DNAAF4-CCPG1, 475 more genes
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