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Items: 1 to 20 of 341

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112762copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 88,973,122-88,979,275 , GRCh38.p12 chr4: 88,051,970-88,058,123 PKD2
    nsv5907258copy number variation1nstd209human GRCh38 chr4: 87,165,110-92,683,258 , GRCh37.p13 chr4: 88,086,262-93,604,409 HSP90AB3P, SPP1, 61 more genes
    nsv5898047copy number variation1nstd209human GRCh38 chr4: 88,071,020-88,086,646 , GRCh37.p13 chr4: 88,992,172-89,007,798 PKD2
    nsv5891587copy number variation1nstd209human GRCh38 chr4: 88,005,818-88,005,897 , GRCh37.p13 chr4: 88,926,970-88,927,049 PKD2
    nsv5840428copy number variation1nstd209human GRCh38 chr4: 88,071,015-88,086,468 , GRCh37.p13 chr4: 88,992,167-89,007,620 PKD2
    nsv5675706mobile element insertion1nstd211human GRCh38 chr4: 88,028,797-88,028,797 , GRCh37.p13 chr4: 88,949,949-88,949,949 PKD2
    nsv5673736copy number variation1nstd102humanPathogenic GRCh37 chr4: 88,984,922-88,989,952 , GRCh38 chr4: 88,063,770-88,068,800 PKD2
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5462834copy number variation1nstd206human GRCh38 chr4: 88,027,322-88,028,482 , GRCh37.p13 chr4: 88,948,474-88,949,634 PKD2
    nsv5456624copy number variation1nstd206human GRCh38 chr4: 88,077,673-88,081,132 , GRCh37.p13 chr4: 88,998,825-89,002,284 PKD2
    nsv5398061mobile element insertion1nstd206human GRCh38 chr4: 88,028,797-88,028,848 , GRCh37.p13 chr4: 88,949,949-88,950,000 PKD2
    nsv5331689translocation1nstd200human GRCh37 chr4: 88,973,296-88,973,296 , GRCh37 chr4: 89,042,162-89,042,162 , GRCh38.p12 chr4: 88,052,144-88,052,144 , GRCh38.p12 chr4: 88,121,010-88,121,010 ABCG2, PKD2
    nsv5317388copy number variation1nstd204human GRCh38.p13 chr4: 88,077,650-88,081,153 , GRCh37.p13 chr4: 88,998,802-89,002,305 PKD2
    nsv5307812copy number variation1nstd204human GRCh38.p13 chr4: 88,027,292-88,028,504 , GRCh37.p13 chr4: 88,948,444-88,949,656 PKD2
    nsv5229917copy number variation1nstd204human GRCh38.p13 chr4: 88,077,701-88,081,100 , GRCh37.p13 chr4: 88,998,853-89,002,252 PKD2
    nsv5228125copy number variation1nstd204human GRCh38.p13 chr4: 88,077,685-88,081,161 , GRCh37.p13 chr4: 88,998,837-89,002,313 PKD2
    nsv5223708copy number variation1nstd204human GRCh38.p13 chr4: 88,027,334-88,028,483 , GRCh37.p13 chr4: 88,948,486-88,949,635 PKD2
    nsv5200857mobile element deletion1nstd204human GRCh38.p13 chr4: 88,024,864-88,025,190 , GRCh37.p13 chr4: 88,946,016-88,946,342 PKD2
    nsv5166227mobile element insertion1nstd203human GRCh38 chr4: 88,034,728-88,034,747 , GRCh37.p13 chr4: 88,955,880-88,955,899 PKD2
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