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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6128469insertion1nstd186human GRCh37 chr3: 57,564,192-57,564,192 , GRCh38.p12 chr3: 57,578,465-57,578,465 ARF4, PDE12
    nsv5970656inversion1nstd209human GRCh38 chr3: 57,602,971-58,277,049 , GRCh37.p13 chr3: 57,588,698-58,262,776 DNASE1L3, FLNB, 12 more genes
    nsv5949954insertion1nstd209human GRCh38 chr3: 57,578,465-57,578,465 , GRCh37.p13 chr3: 57,564,192-57,564,192 PDE12, ARF4
    nsv5900789copy number variation1nstd209human GRCh38 chr3: 57,589,215-57,592,918 , GRCh37.p13 chr3: 57,574,942-57,578,645 PDE12, ARF4
    nsv5892440copy number variation1nstd209human GRCh38 chr3: 57,573,624-57,573,984 , GRCh37.p13 chr3: 57,559,351-57,559,711 ARF4, PDE12
    nsv5836689copy number variation1nstd209human GRCh38 chr3: 57,603,037-57,611,113 , GRCh37.p13 chr3: 57,588,764-57,596,840 PDE12
    nsv5836086copy number variation2nstd209human GRCh38 chr3: 57,605,537-57,606,536 , GRCh37.p13 chr3: 57,591,264-57,592,263 PDE12
    nsv5836085copy number variation1nstd209human GRCh38 chr3: 57,589,242-57,592,908 , GRCh37.p13 chr3: 57,574,969-57,578,635 ARF4, PDE12
    nsv5730851mobile element insertion1nstd211human GRCh38 chr3: 57,613,152-57,613,152 , GRCh37.p13 chr3: 57,598,879-57,598,879 PDE12
    nsv5725914mobile element insertion1nstd211human GRCh38 chr3: 57,592,078-57,592,078 , GRCh37.p13 chr3: 57,577,805-57,577,805 ARF4, PDE12
    nsv5716484mobile element insertion1nstd211human GRCh38 chr3: 57,602,974-57,602,974 , GRCh37.p13 chr3: 57,588,701-57,588,701 PDE12
    nsv5689505mobile element insertion2nstd211human GRCh38 chr3: 57,578,473-57,578,473 , GRCh37.p13 chr3: 57,564,200-57,564,200 PDE12, ARF4
    nsv5681898mobile element insertion2nstd211human GRCh38 chr3: 57,639,812-57,639,812 , GRCh37.p13 chr3: 57,625,539-57,625,539 PDE12, DENND6A
    nsv5676275mobile element insertion1nstd211human GRCh38 chr3: 57,625,728-57,625,728 , GRCh37.p13 chr3: 57,611,455-57,611,455 PDE12, DENND6A
    nsv5613111insertion1nstd207human GRCh38 chr3: 57,644,752-57,644,752 , GRCh37.p13 chr3: 57,630,479-57,630,479 PDE12, DENND6A
    nsv5608088insertion1nstd207human GRCh38 chr3: 57,639,800-57,639,800 , GRCh37.p13 chr3: 57,625,527-57,625,527 PDE12, DENND6A
    nsv5606547insertion1nstd207human GRCh38 chr3: 57,578,465-57,578,465 , GRCh37.p13 chr3: 57,564,192-57,564,192 PDE12, ARF4
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 more genes
    nsv5540608insertion1nstd206human GRCh38 chr3: 57,627,478-57,627,478 , GRCh37.p13 chr3: 57,613,205-57,613,205 PDE12, DENND6A
    nsv5536469insertion1nstd206human GRCh38 chr3: 57,578,465-57,578,465 , GRCh37.p13 chr3: 57,564,192-57,564,192 ARF4, PDE12
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