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Items: 1 to 20 of 321

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904284copy number variation1nstd209human GRCh38 chr4: 168,316,101-168,316,178 , GRCh37.p13 chr4: 169,237,252-169,237,329 DDX60
    nsv5898913copy number variation1nstd209human GRCh38 chr4: 168,263,499-168,263,665 , GRCh37.p13 chr4: 169,184,650-169,184,816 DDX60
    nsv5893021copy number variation1nstd209human GRCh38 chr4: 168,297,269-168,297,333 , GRCh37.p13 chr4: 169,218,420-169,218,484 DDX60
    nsv5692217mobile element insertion2nstd211human GRCh38 chr4: 168,263,327-168,263,327 , GRCh37.p13 chr4: 169,184,478-169,184,478 DDX60
    nsv5634471insertion1nstd207human GRCh38 chr4: 168,297,382-168,297,382 , GRCh37.p13 chr4: 169,218,533-169,218,533 DDX60
    nsv5631033insertion1nstd207human GRCh38 chr4: 168,243,865-168,243,865 , GRCh37.p13 chr4: 169,165,016-169,165,016 DDX60
    nsv5572500copy number variation1nstd207human GRCh38 chr4: 168,297,332-168,297,381 , GRCh37.p13 chr4: 169,218,483-169,218,532 DDX60
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5546219insertion1nstd206human GRCh38 chr4: 168,285,744-168,285,758 , GRCh37.p13 chr4: 169,206,895-169,206,909 DDX60
    nsv5534473insertion1nstd206human GRCh38 chr4: 168,285,670-168,285,750 , GRCh37.p13 chr4: 169,206,821-169,206,901 DDX60
    nsv5466965copy number variation1nstd206human GRCh38 chr4: 168,043,588-168,644,848 , GRCh37.p13 chr4: 168,964,739-169,565,999 ANXA10, PALLD, 5 more genes
    nsv5466891copy number variation1nstd206human GRCh38 chr4: 168,264,248-168,265,039 , GRCh37.p13 chr4: 169,185,399-169,186,190 DDX60
    nsv5458929copy number variation1nstd206human GRCh38 chr4: 168,278,523-168,278,944 , GRCh37.p13 chr4: 169,199,674-169,200,095 DDX60
    nsv5397927mobile element insertion1nstd206human GRCh38 chr4: 168,263,327-168,263,378 , GRCh37.p13 chr4: 169,184,478-169,184,529 DDX60
    nsv5381776copy number variation1nstd102humanPathogenic GRCh37 chr4: 157,771,352-172,496,278 , GRCh38.p12 chr4: 156,850,200-171,575,127 LOC107986326, LOC107986240, 144 more genes
    nsv5353455translocation1nstd200human GRCh38 chr4: 168,263,499-168,263,499 , GRCh38 chr4: 168,263,670-168,263,670 , GRCh37.p13 chr4: 169,184,650-169,184,650 , GRCh37.p13 chr4: 169,184,821-169,184,821 DDX60
    nsv5353454translocation1nstd200human GRCh38 chr4: 168,252,395-168,252,395 , GRCh38 chr4: 168,252,453-168,252,453 , GRCh37.p13 chr4: 169,173,604-169,173,604 , GRCh37.p13 chr4: 169,173,546-169,173,546 DDX60
    nsv5344141translocation1nstd200human GRCh37 chr4: 169,184,650-169,184,650 , GRCh37 chr4: 169,184,821-169,184,821 , GRCh38.p12 chr4: 168,263,499-168,263,499 , GRCh38.p12 chr4: 168,263,670-168,263,670 DDX60
    nsv5175130mobile element insertion1nstd203human GRCh38 chr4: 168,243,865-168,243,879 , GRCh37.p13 chr4: 169,165,016-169,165,030 DDX60
    nsv5095721mobile element insertion1nstd203human GRCh38 chr4: 168,243,865-168,243,879 , GRCh37.p13 chr4: 169,165,016-169,165,030 DDX60
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