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Items: 1 to 20 of 1043

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144578insertion1nstd232human GRCh37.p13 chr5: 78,035,992-78,035,992 , GRCh38.p12 chr5: 78,740,169-78,740,169 LHFPL2
    nsv7096788copy number variation1nstd102humanPathogenic GRCh37 chr5: 76,115,008-78,281,071 , GRCh38.p12 chr5: 76,819,183-78,985,248 LHFPL2, OTP, 27 more genes
    nsv7055091inversion1nstd229human GRCh38 chr5: 78,613,589-78,618,617 , GRCh37.p13 chr5: 77,909,412-77,914,440 LHFPL2
    nsv7050643inversion1nstd229human GRCh38 chr5: 77,339,476-78,646,078 , GRCh37.p13 chr5: 76,635,301-77,941,901 LHFPL2, RNU6-183P, 15 more genes
    nsv7050159inversion1nstd229human GRCh38 chr5: 78,534,401-78,548,668 , GRCh37.p13 chr5: 77,830,224-77,844,491 LHFPL2
    nsv7045119inversion1nstd229human GRCh38 chr5: 76,735,197-79,503,040 , GRCh37.p13 chr5: 76,031,022-78,798,863 RNU6ATAC36P, RPS3AP20, 39 more genes
    nsv7041510inversion1nstd229human GRCh38 chr5: 73,610,616-81,398,473 , GRCh37.p13 chr5: 72,906,441-80,694,292 LOC105379034, RBMX2P5, 134 more genes
    nsv7040742inversion1nstd229human GRCh38 chr5: 78,500,374-78,510,627 , GRCh37.p13 chr5: 77,796,197-77,806,450 LHFPL2
    nsv7039910inversion1nstd229human GRCh38 chr5: 78,582,950-78,866,961 , GRCh37.p13 chr5: 77,878,773-78,162,784 LHFPL2, HMGB1P21, 1 more genes
    nsv7038776inversion1nstd229human GRCh38 chr5: 76,735,364-79,502,930 , GRCh37.p13 chr5: 76,031,189-78,798,753 HOMER1, LOC100505796, 39 more genes
    nsv7038577inversion1nstd229human GRCh38 chr5: 78,653,556-78,654,393 , GRCh37.p13 chr5: 77,949,379-77,950,216 LHFPL2
    nsv6777685copy number variation1nstd229human GRCh38 chr5: 78,695,465-78,700,305 , GRCh37.p13 chr5: 77,991,288-77,996,128 LHFPL2
    nsv6777560copy number variation1nstd229human GRCh38 chr5: 78,491,201-78,548,400 , GRCh37.p13 chr5: 77,787,024-77,844,223 LHFPL2
    nsv6776687copy number variation1nstd229human GRCh38 chr5: 78,760,001-78,763,900 , GRCh37.p13 chr5: 78,055,824-78,059,723 LHFPL2
    nsv6776514copy number variation1nstd229human GRCh38 chr5: 78,585,988-78,591,923 , GRCh37.p13 chr5: 77,881,811-77,887,746 LHFPL2
    nsv6776466copy number variation1nstd229human GRCh38 chr5: 78,652,401-78,657,500 , GRCh37.p13 chr5: 77,948,224-77,953,323 LHFPL2
    nsv6775987copy number variation1nstd229human GRCh38 chr5: 78,623,235-78,623,394 , GRCh37.p13 chr5: 77,919,058-77,919,217 LHFPL2
    nsv6775864copy number variation1nstd229human GRCh38 chr5: 78,579,435-78,619,546 , GRCh37.p13 chr5: 77,875,258-77,915,369 LHFPL2
    nsv6774976copy number variation1nstd229human GRCh38 chr5: 78,759,787-78,761,155 , GRCh37.p13 chr5: 78,055,610-78,056,978 LHFPL2
    nsv6774886copy number variation1nstd229human GRCh38 chr5: 78,692,827-78,697,249 , GRCh37.p13 chr5: 77,988,650-77,993,072 LHFPL2
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