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Items: 1 to 20 of 544

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6120094copy number variation1nstd186human GRCh37 chr4: 21,716,466-21,716,673 , GRCh38.p12 chr4: 21,714,843-21,715,050 , GRCh38.p12 chr4|NT_187540.1: 200,679-200,886 KCNIP4
    nsv5341975translocation1nstd200human GRCh37 chr4: 21,694,730-21,694,730 , GRCh37 chr4: 21,694,850-21,694,850 , GRCh38.p12 chr4|NT_187540.1: 178,943-178,943 , GRCh38.p12 chr4|NT_187540.1: 179,063-179,063 , GRCh38.p12 chr4: 21,693,107-21,693,107 , GRCh38.p12 chr4: 21,693,227-21,693,227 KCNIP4
    nsv4809087copy number variation1nstd200human GRCh37 chr4: 21,662,679-21,662,945 , GRCh38.p12 chr4|NT_187540.1: 146,892-147,158 , GRCh38.p12 chr4: 21,661,056-21,661,322 , KCNIP4
    nsv4799711copy number variation1nstd200human GRCh37 chr4: 21,676,456-21,676,632 , GRCh38.p12 chr4: 21,674,833-21,675,009 , GRCh38.p12 chr4|NT_187540.1: 160,669-160,845 , KCNIP4
    nsv4799710copy number variation1nstd200human GRCh37 chr4: 21,590,771-21,590,910 , GRCh38.p12 chr4: 21,589,148-21,589,287 , GRCh38.p12 chr4|NT_187540.1: 67,818-67,987 KCNIP4, LOC105374516
    nsv4799709copy number variation1nstd200human GRCh37 chr4: 21,587,817-21,592,844 , GRCh38.p12 chr4: 21,586,194-21,591,221 , GRCh38.p12 chr4|NT_187540.1: 64,870-69,921 KCNIP4, LOC105374516
    nsv4799708copy number variation1nstd200human GRCh37 chr4: 21,543,741-21,566,298 , GRCh38.p12 chr4|NT_187540.1: 20,752-43,309 , GRCh38.p12 chr4: 21,542,118-21,564,675 KCNIP4
    nsv4799707copy number variation1nstd200human GRCh37 chr4: 21,517,511-21,581,329 , GRCh38.p12 chr4: 21,515,888-21,579,706 , GRCh38.p12 chr4|NT_187540.1: 1-58,337 KCNIP4
    nsv4766015insertion1nstd199human GRCh37 chr4: 21,635,651-21,635,651 , GRCh38.p12 chr4|NT_187540.1: 119,864-119,864 , GRCh38.p12 chr4: 21,634,028-21,634,028 KCNIP4
    nsv4754005insertion1nstd199human GRCh37 chr4: 21,534,588-21,534,588 , GRCh38.p12 chr4: 21,532,965-21,532,965 , GRCh38.p12 chr4|NT_187540.1: 11,599-11,599 KCNIP4
    nsv4742786copy number variation1nstd199human GRCh37 chr4: 21,716,406-21,716,503 , GRCh38.p12 chr4: 21,714,783-21,714,880 , GRCh38.p12 chr4|NT_187540.1: 200,619-200,716 KCNIP4
    nsv4733619copy number variation1nstd199human GRCh37 chr4: 21,694,729-21,694,847 , GRCh38.p12 chr4|NT_187540.1: 178,942-179,060 , GRCh38.p12 chr4: 21,693,106-21,693,224 KCNIP4
    nsv4732194copy number variation1nstd199human GRCh37 chr4: 21,530,309-21,530,366 , GRCh38.p12 chr4|NT_187540.1: 7,320-7,377 , GRCh38.p12 chr4: 21,528,686-21,528,743 KCNIP4
    nsv4720230insertion1nstd186human GRCh37 chr4: 21,534,572-21,534,572 , GRCh38.p12 chr4: 21,532,949-21,532,949 , GRCh38.p12 chr4|NT_187540.1: 11,583-11,583 KCNIP4
    nsv4699174mobile element insertion2nstd186human GRCh37 chr4: 21,596,435-21,596,435 , GRCh38.p12 chr4: 21,594,812-21,594,812 , GRCh38.p12 chr4|NT_187540.1: 73,527-73,527 KCNIP4, LOC105374516
    nsv4686071mobile element insertion1nstd186human GRCh37 chr4: 21,534,589-21,534,589 , GRCh38.p12 chr4: 21,532,966-21,532,966 , GRCh38.p12 chr4|NT_187540.1: 11,600-11,600 KCNIP4
    nsv4679170copy number variation1nstd189human GRCh37.p13 chr4: 21,555,308-21,833,671 , GRCh38.p12 chr4: 21,553,685-21,832,048 , GRCh38.p12 chr4|NT_187540.1: 32,319-220,246 , KCNIP4, 2 more genes
    nsv4638259copy number variation2nstd186human GRCh37 chr4: 21,694,730-21,694,850 , GRCh38.p12 chr4: 21,693,107-21,693,227 , GRCh38.p12 chr4|NT_187540.1: 178,943-179,063 KCNIP4
    nsv4597190copy number variation1nstd183human GRCh37 chr4: 21,672,928-21,688,216 , GRCh38.p12 chr4: 21,671,305-21,686,593 , GRCh38.p12 chr4|NT_187540.1: 157,141-172,429 , KCNIP4
    nsv4597189copy number variation1nstd183human GRCh37 chr4: 21,543,815-21,566,178 , GRCh38.p12 chr4|NT_187540.1: 20,826-43,189 , GRCh38.p12 chr4: 21,542,192-21,564,555 KCNIP4
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