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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057419inversion1nstd229human GRCh38 chr3: 142,194,277-142,443,354 , GRCh37.p13 chr3: 141,913,119-142,162,196 RNU6-1294P, RNU1-100P, 2 more genes
    nsv7053869inversion1nstd229human GRCh38 chr3: 142,150,470-142,156,818 , GRCh37.p13 chr3: 141,869,312-141,875,660 GK5
    nsv7051991inversion1nstd229human GRCh38 chr3: 142,222,793-142,222,844 , GRCh37.p13 chr3: 141,941,635-141,941,686 GK5
    nsv6737691copy number variation1nstd229human GRCh38 chr3: 142,148,501-142,204,500 , GRCh37.p13 chr3: 141,867,343-141,923,342 GK5, TFDP2
    nsv6733049copy number variation1nstd229human GRCh38 chr3: 142,172,035-142,172,130 , GRCh37.p13 chr3: 141,890,877-141,890,972 GK5
    nsv6731755copy number variation1nstd229human GRCh38 chr3: 141,757,101-142,395,000 , GRCh37.p13 chr3: 141,475,943-142,113,842 RNU6-509P, RNU6-425P, 8 more genes
    nsv6730730copy number variation1nstd229human GRCh38 chr3: 142,199,756-142,202,839 , GRCh37.p13 chr3: 141,918,598-141,921,681 GK5
    nsv6729221copy number variation1nstd229human GRCh38 chr3: 142,197,182-142,199,440 , GRCh37.p13 chr3: 141,916,024-141,918,282 GK5
    nsv6727341copy number variation1nstd229human GRCh38 chr3: 142,107,101-142,349,700 , GRCh37.p13 chr3: 141,825,943-142,068,542 GK5, XRN1, 2 more genes
    nsv6722346copy number variation1nstd229human GRCh38 chr3: 142,160,720-142,161,264 , GRCh37.p13 chr3: 141,879,562-141,880,106 GK5
    nsv6721161copy number variation1nstd229human GRCh38 chr3: 142,159,620-142,162,803 , GRCh37.p13 chr3: 141,878,462-141,881,645 GK5
    nsv6720265copy number variation1nstd229human GRCh38 chr3: 142,187,710-142,193,335 , GRCh37.p13 chr3: 141,906,552-141,912,177 GK5
    nsv6718565copy number variation1nstd229human GRCh38 chr3: 142,194,301-142,373,200 , GRCh37.p13 chr3: 141,913,143-142,092,042 GK5, XRN1
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6628694copy number variation15nstd224human GRCh37 chr3: 141,845,000-142,085,310 , GRCh38.p12 chr3: 142,126,158-142,366,468 RNU6-425P, TFDP2, 2 more genes
    nsv6628693copy number variation1nstd224human GRCh37 chr3: 141,845,000-142,051,882 , GRCh38.p12 chr3: 142,126,158-142,333,040 XRN1, RNU6-425P, 2 more genes
    nsv6628692copy number variation1nstd224human GRCh37 chr3: 141,809,984-142,085,310 , GRCh38.p12 chr3: 142,091,142-142,366,468 XRN1, GK5, 2 more genes
    nsv6628646copy number variation1nstd224human GRCh37 chr3: 141,845,000-142,103,365 , GRCh38.p12 chr3: 142,126,158-142,384,523 TFDP2, RNU6-425P, 2 more genes
    nsv6628645copy number variation2nstd224human GRCh37 chr3: 141,845,000-142,084,168 , GRCh38.p12 chr3: 142,126,158-142,365,326 TFDP2, RNU6-425P, 2 more genes
    nsv6628644copy number variation2nstd224human GRCh37 chr3: 141,824,924-142,080,063 , GRCh38.p12 chr3: 142,106,082-142,361,221 RNU6-425P, TFDP2, 2 more genes
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