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Items: 1 to 20 of 187

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057064inversion1nstd229human GRCh38 chr4: 139,224,189-139,637,638 , GRCh37.p13 chr4: 140,145,343-140,558,792 RAB33B, LOC105377451, 13 more genes
    nsv7045068inversion1nstd229human GRCh38 chr4: 138,588,072-141,319,129 , GRCh37.p13 chr4: 139,509,226-142,240,283 RN7SKP253, FTH1P24, 41 more genes
    nsv6756952copy number variation1nstd229human GRCh38 chr4: 139,454,381-139,498,894 , GRCh37.p13 chr4: 140,375,535-140,420,048 RAB33B-AS1, SETD7, 1 more genes
    nsv6756866copy number variation1nstd229human GRCh38 chr4: 139,449,515-139,455,138 , GRCh37.p13 chr4: 140,370,669-140,376,292 RAB33B, RAB33B-AS1
    nsv6753187copy number variation1nstd229human GRCh38 chr4: 139,464,901-139,467,100 , GRCh37.p13 chr4: 140,386,055-140,388,254 RAB33B
    nsv6750669copy number variation1nstd229human GRCh38 chr4: 139,455,030-139,463,420 , GRCh37.p13 chr4: 140,376,184-140,384,574 RAB33B
    nsv6748510copy number variation1nstd229human GRCh38 chr4: 139,456,901-139,462,100 , GRCh37.p13 chr4: 140,378,055-140,383,254 RAB33B
    nsv6744278copy number variation1nstd229human GRCh38 chr4: 139,457,135-139,457,436 , GRCh37.p13 chr4: 140,378,289-140,378,590 RAB33B
    nsv6740407copy number variation1nstd229human GRCh38 chr4: 139,467,356-139,471,176 , GRCh37.p13 chr4: 140,388,510-140,392,330 RAB33B
    nsv6629166copy number variation1nstd224human GRCh37 chr4: 140,292,217-140,614,711 , GRCh38.p12 chr4: 139,371,063-139,693,557 MGST2, NAA15, 9 more genes
    nsv6566156inversion1nstd223human GRCh38 chr4: 139,467,202-139,467,622 , GRCh37.p13 chr4: 140,388,356-140,388,776 RAB33B
    nsv6380427copy number variation1nstd223human GRCh38 chr4: 139,467,356-139,471,185 , GRCh37.p13 chr4: 140,388,510-140,392,339 RAB33B
    nsv6313878copy number variation1nstd102humanPathogenic GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443 LINC00613, GYPA, 448 more genes
    nsv6313656copy number variation1nstd102humanUncertain significance GRCh37 chr4: 136,035,308-144,718,930 , GRCh38.p12 chr4: 135,114,153-143,797,777 RPS2P20, LOC105377444, 87 more genes
    nsv6311714copy number variation1nstd102humanUncertain significance GRCh37 chr4: 140,375,350-140,375,618 , GRCh38.p12 chr4: 139,454,196-139,454,464 RAB33B, RAB33B-AS1
    nsv6311713copy number variation1nstd102humanUncertain significance GRCh37 chr4: 140,222,932-140,394,280 , GRCh38.p12 chr4: 139,301,778-139,473,126 NDUFC1, NAA15, 4 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6291168copy number variation1nstd102humanPathogenic GRCh37 chr4: 138,289,049-145,923,298 , GRCh38.p12 chr4: 137,367,895-145,002,146 LOC105377447, RN7SKP253, 92 more genes
    nsv6290718copy number variation1nstd102humanPathogenic GRCh37 chr4: 136,529,470-141,564,812 , GRCh38.p12 chr4: 135,608,315-140,643,658 MGARP, NAA15, 61 more genes
    nsv6134893copy number variation1nstd213human GRCh37 chr4: 140,230,000-141,060,001 , GRCh38.p12 chr4: 139,308,846-140,138,847 MGST2, MAML3, 15 more genes
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