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Items: 1 to 20 of 203

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5961126insertion1nstd209human GRCh38 chr6: 116,729,208-116,729,208 , GRCh37.p13 chr6: 117,050,371-117,050,371 KPNA5
    nsv5901874copy number variation1nstd209human GRCh38 chr6: 116,721,047-116,721,125 , GRCh37.p13 chr6: 117,042,210-117,042,288 KPNA5
    nsv5729226mobile element insertion1nstd211human GRCh38 chr6: 116,715,187-116,715,187 , GRCh37.p13 chr6: 117,036,350-117,036,350 KPNA5
    nsv5688792mobile element insertion1nstd211human GRCh38 chr6: 116,695,886-116,695,886 , GRCh37.p13 chr6: 117,017,049-117,017,049 KPNA5
    nsv5562339mobile element insertion1nstd206human GRCh38 chr6: 116,715,187-116,715,238 , GRCh37.p13 chr6: 117,036,350-117,036,401 KPNA5
    nsv5399225mobile element insertion1nstd206human GRCh38 chr6: 116,695,886-116,695,937 , GRCh37.p13 chr6: 117,017,049-117,017,100 KPNA5
    nsv5369660translocation1nstd200human GRCh38 chr6: 116,695,662-116,695,662 , GRCh38 chr6: 116,695,589-116,695,589 , GRCh37.p13 chr6: 117,016,752-117,016,752 , GRCh37.p13 chr6: 117,016,825-117,016,825 KPNA5
    nsv5345322translocation1nstd200human GRCh37 chr6: 117,016,752-117,016,752 , GRCh37 chr6: 117,016,825-117,016,825 , GRCh38.p12 chr6: 116,695,589-116,695,589 , GRCh38.p12 chr6: 116,695,662-116,695,662 KPNA5
    nsv5240360copy number variation1nstd204human GRCh38.p13 chr6: 116,731,901-116,736,400 , GRCh37.p13 chr6: 117,053,064-117,057,563 KPNA5
    nsv5100809mobile element insertion1nstd203human GRCh38 chr6: 116,731,238-116,731,252 , GRCh37.p13 chr6: 117,052,401-117,052,415 KPNA5
    nsv5038830inversion1nstd200human GRCh38 chr6: 84,210,829-134,196,676 , GRCh37.p13 chr6: 84,920,547-134,517,814 , LOC105377981, 623 more genes
    nsv4948357copy number variation1nstd200human GRCh38 chr6: 116,740,103-116,742,393 , GRCh37.p13 chr6: 117,061,266-117,063,556 KPNA5
    nsv4948356copy number variation1nstd200human GRCh38 chr6: 116,736,909-116,748,212 , GRCh37.p13 chr6: 117,058,072-117,069,375 KPNA5
    nsv4945593copy number variation1nstd200human GRCh38 chr6: 116,730,734-116,742,865 , GRCh37.p13 chr6: 117,051,897-117,064,028 KPNA5
    nsv4817655copy number variation1nstd200human GRCh37 chr6: 117,061,266-117,063,553 , GRCh38.p12 chr6: 116,740,103-116,742,390 KPNA5
    nsv4768325copy number variation1nstd102humanPathogenic GRCh37 chr6: 116,734,559-123,648,104 , GRCh38.p12 chr6: 116,413,396-123,326,959 GJA1, RNU4-76P, 80 more genes
    nsv4729289copy number variation1nstd102humanUncertain significance GRCh37 chr6: 116,978,714-117,537,404 , GRCh38.p12 chr6: 116,657,551-117,216,241 KPNA5, GPRC6A, 6 more genes
    nsv4685989copy number variation1nstd102humanPathogenic GRCh37 chr6: 101,287,058-117,013,245 , GRCh38.p12 chr6: 100,839,182-116,692,082 RPL23AP50, RNU6-960P, 216 more genes
    nsv4606056copy number variation1nstd183human GRCh37 chr6: 117,016,528-117,020,017 , GRCh38.p12 chr6: 116,695,365-116,698,854 KPNA5
    nsv4602288copy number variation1nstd183human GRCh37 chr6: 117,050,969-117,062,299 , GRCh38.p12 chr6: 116,729,806-116,741,136 KPNA5
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