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Items: 1 to 20 of 307

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6127133insertion1nstd186human GRCh37 chr4: 66,802,481-66,802,481 , GRCh38.p12 chr4|NW_013171800.1: 56,315-56,315 , GRCh38.p12 chr4: 65,936,763-65,936,763 0
    nsv5385416mobile element deletion2nstd186human GRCh37 chr4: 66,755,390-66,755,655 , GRCh38.p12 chr4: 65,889,672-65,889,937 , GRCh38.p12 chr4|NW_013171800.1: 9,219-9,484 0
    nsv5337376translocation1nstd200human GRCh37 chr4: 66,800,655-66,800,655 , GRCh37 chr4: 66,800,476-66,800,476 , GRCh38.p12 chr4: 65,934,758-65,934,758 , GRCh38.p12 chr4|NW_013171800.1: 54,298-54,298 , GRCh38.p12 chr4|NW_013171800.1: 54,477-54,477 , GRCh38.p12 chr4: 65,934,937-65,934,937 0
    nsv4885370inversion1nstd200human GRCh37 chr4: 66,607,176-66,911,498 , GRCh38.p12 chr4: 65,741,458-66,045,780 , GRCh38.p12 chr4|NW_013171800.1: 1-163,749 LOC105377258, LOC105377259, 3 more genes
    nsv4800013copy number variation1nstd200human GRCh37 chr4: 66,897,421-66,897,532 , GRCh38.p12 chr4: 66,031,703-66,031,814 , GRCh38.p12 chr4|NW_013171800.1: 155,175-155,286 LOC105377261
    nsv4800012copy number variation1nstd200human GRCh37 chr4: 66,892,837-66,897,374 , GRCh38.p12 chr4: 66,027,119-66,031,656 , GRCh38.p12 chr4|NW_013171800.1: 150,591-155,128 LOC105377261
    nsv4800011copy number variation1nstd200human GRCh37 chr4: 66,837,698-66,837,840 , GRCh38.p12 chr4: 65,971,980-65,972,122 , GRCh38.p12 chr4|NW_013171800.1: 95,452-95,594 0
    nsv4800010copy number variation1nstd200human GRCh37 chr4: 66,829,451-66,951,198 , GRCh38.p12 chr4: 65,963,733-66,085,480 , GRCh38.p12 chr4|NW_013171800.1: 87,205-163,749 LOC105377261
    nsv4800009copy number variation1nstd200human GRCh37 chr4: 66,817,732-66,819,577 , GRCh38.p12 chr4: 65,952,014-65,953,859 , GRCh38.p12 chr4|NW_013171800.1: 75,486-77,331 0
    nsv4800008copy number variation1nstd200human GRCh37 chr4: 66,807,494-66,808,872 , GRCh38.p12 chr4|NW_013171800.1: 65,248-66,626 , GRCh38.p12 chr4: 65,941,776-65,943,154 LOC105377260
    nsv4800007copy number variation1nstd200human GRCh37 chr4: 66,802,606-66,807,164 , GRCh38.p12 chr4: 65,936,888-65,941,446 , GRCh38.p12 chr4|NW_013171800.1: 60,583-64,918 0
    nsv4778065mobile element deletion1nstd200human GRCh37 chr4: 66,755,390-66,755,655 , GRCh38.p12 chr4|NW_013171800.1: 9,219-9,484 , GRCh38.p12 chr4: 65,889,672-65,889,937 0
    nsv4755272insertion1nstd199human GRCh37 chr4: 66,802,474-66,802,474 , GRCh38.p12 chr4|NW_013171800.1: 56,308-56,308 , GRCh38.p12 chr4: 65,936,756-65,936,756 0
    nsv4753454insertion1nstd199human GRCh37 chr4: 66,809,072-66,809,072 , GRCh38.p12 chr4: 65,943,354-65,943,354 , GRCh38.p12 chr4|NW_013171800.1: 66,826-66,826 LOC105377260
    nsv4738113copy number variation1nstd199human GRCh37 chr4: 66,755,382-66,755,662 , GRCh38.p12 chr4|NW_013171800.1: 9,211-9,491 , GRCh38.p12 chr4: 65,889,664-65,889,944 0
    nsv4721574mobile element insertion1nstd186human GRCh37 chr4: 66,809,078-66,809,078 , GRCh38.p12 chr4|NW_013171800.1: 66,832-66,832 , GRCh38.p12 chr4: 65,943,360-65,943,360 LOC105377260
    nsv4719866insertion1nstd186human GRCh37 chr4: 66,832,657-66,832,657 , GRCh38.p12 chr4: 65,966,939-65,966,939 , GRCh38.p12 chr4|NW_013171800.1: 90,411-90,411 0
    nsv4700735mobile element insertion1nstd186human GRCh37 chr4: 66,809,081-66,809,081 , GRCh38.p12 chr4: 65,943,363-65,943,363 , GRCh38.p12 chr4|NW_013171800.1: 66,835-66,835 LOC105377260
    nsv4645660mobile element deletion1nstd186human GRCh37 chr4: 66,755,376-66,755,655 , GRCh38.p12 chr4|NW_013171800.1: 9,205-9,484 , GRCh38.p12 chr4: 65,889,658-65,889,937 0
    nsv4635597copy number variation2nstd186human GRCh37 chr4: 66,755,390-66,755,655 , GRCh38.p12 chr4|NW_013171800.1: 9,219-9,484 , GRCh38.p12 chr4: 65,889,672-65,889,937 0
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