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Items: 1 to 20 of 1766

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6126416insertion1nstd186human GRCh37 chr4: 190,819,056-190,819,122 , GRCh38.p12 chr4: 189,897,901-189,897,967 , GRCh38.p12 chr4|NT_187679.1: 546,630-546,696 , GRCh38.p12 chr4|NT_187543.1: 234,927-234,993 , GRCh38.p12 chr4|NT_187650.1: 235,410-235,476 FRG1-DT
    nsv5968482inversion1nstd209human GRCh38 chr4: 188,099,102-189,888,437 , GRCh37.p13 chr4: 189,020,256-190,809,592 HSP90AA4P, RPL7AP27, 27 more genes
    nsv5952447insertion1nstd209human GRCh38 chr4: 189,858,944-189,858,944 , GRCh37.p13 chr4: 190,780,099-190,780,099 FRG1-DT
    nsv5902490copy number variation1nstd209human GRCh38 chr4: 189,835,800-189,837,254 , GRCh37.p13 chr4: 190,756,955-190,758,409 FRG1-DT
    nsv5899414copy number variation1nstd209human GRCh38 chr4: 189,810,576-189,810,982 , GRCh37.p13 chr4: 190,731,730-190,732,136 FRG1-DT, LOC105377619
    nsv5898064copy number variation1nstd209human GRCh38 chr4: 189,905,613-189,905,727 , GRCh37.p13 chr4: 190,826,768-190,826,882 FRG1-DT
    nsv5896709copy number variation1nstd209human GRCh38 chr4: 189,793,804-189,797,274 , GRCh37.p13 chr4: 190,714,958-190,718,428 FRG1-DT
    nsv5896448copy number variation1nstd209human GRCh38 chr4: 189,835,805-189,837,108 , GRCh37.p13 chr4: 190,756,960-190,758,263 FRG1-DT
    nsv5894362copy number variation1nstd209human GRCh38 chr4: 189,925,247-189,926,201 , GRCh37.p13 chr4|NW_003571034.1: 18,177-19,131 FRG1-DT
    nsv5892191copy number variation1nstd209human GRCh38 chr4: 189,813,108-189,817,468 , GRCh37.p13 chr4: 190,734,262-190,738,622 LOC105377619, FRG1-DT
    nsv5891321copy number variation1nstd209human GRCh38 chr4: 189,835,681-189,835,900 , GRCh37.p13 chr4: 190,756,836-190,757,055 FRG1-DT
    nsv5889792copy number variation1nstd209human GRCh38 chr4: 189,820,301-189,820,642 , GRCh37.p13 chr4: 190,741,455-190,741,796 LOC105377619, FRG1-DT
    nsv5888838copy number variation1nstd209human GRCh38 chr4: 189,837,378-189,837,444 , GRCh37.p13 chr4: 190,758,533-190,758,599 FRG1-DT
    nsv5888149copy number variation1nstd209human GRCh38 chr4: 189,840,532-189,840,604 , GRCh37.p13 chr4: 190,761,687-190,761,759 FRG1-DT
    nsv5887611copy number variation1nstd209human GRCh38 chr4: 189,846,048-189,847,005 , GRCh37.p13 chr4: 190,767,203-190,768,160 FRG1-DT
    nsv5839207copy number variation2nstd209human GRCh38 chr4: 189,885,703-189,886,802 , GRCh37.p13 chr4: 190,806,858-190,807,957 FRG1-DT
    nsv5839206copy number variation1nstd209human GRCh38 chr4: 189,873,135-189,875,434 , GRCh37.p13 chr4: 190,794,290-190,796,589 FRG1-DT
    nsv5839205copy number variation3nstd209human GRCh38 chr4: 189,840,009-189,841,508 , GRCh37.p13 chr4: 190,761,164-190,762,663 FRG1-DT
    nsv5839204copy number variation1nstd209human GRCh38 chr4: 189,828,941-189,830,640 , GRCh37.p13 chr4: 190,750,096-190,751,795 FRG1-DT
    nsv5839203copy number variation1nstd209human GRCh38 chr4: 189,762,023-189,763,598 , GRCh37.p13 chr4: 190,683,177-190,684,752 FRG1-DT
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