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Items: 1 to 20 of 170

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097564copy number variation1nstd102humanUncertain significance GRCh37 chr6: 108,197,748-108,395,855 , GRCh38.p12 chr6: 107,876,544-108,074,651 SEC63, OSTM1, 5 more genes
    nsv7097560copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr6: 107,019,871-110,266,416 , GRCh38.p12 chr6: 106,571,996-109,945,213 ZPR1P1, OSTM1, 60 more genes
    nsv7050372inversion1nstd229human GRCh38 chr6: 107,280,655-111,259,922 , GRCh37.p13 chr6: 107,601,859-111,581,125 SNORA40C, PPIL6, 77 more genes
    nsv7044587inversion1nstd229human GRCh38 chr6: 107,042,208-108,316,831 , GRCh37.p13 chr6: 107,495,575-108,638,035 RPL3P7, MTHFD2P3, 19 more genes
    nsv7043260inversion1nstd229human GRCh38 chr6: 107,500,793-111,264,842 , GRCh37.p13 chr6: 107,821,997-111,586,045 ZBTB24-DT, RNU6-906P, 76 more genes
    nsv6815848copy number variation1nstd229human GRCh38 chr6: 108,065,801-108,078,480 , GRCh37.p13 chr6: 108,387,005-108,399,684 OSTM1
    nsv6809159copy number variation1nstd229human GRCh38 chr6: 107,970,989-108,121,645 , GRCh37.p13 chr6: 108,292,193-108,442,849 OSTM1-AS1, LOC105377929, 3 more genes
    nsv6804847copy number variation1nstd229human GRCh38 chr6: 105,481,597-109,225,980 , GRCh37.p13 chr6: 105,929,472-109,547,183 LINC02836, SOBP, 61 more genes
    nsv6800412copy number variation1nstd229human GRCh38 chr6: 108,006,342-108,042,430 , GRCh37.p13 chr6: 108,327,546-108,363,634 OSTM1, LOC105377929
    nsv6637047copy number variation1nstd102humanUncertain significance GRCh37 chr6: 108,189,941-108,498,389 , GRCh38.p12 chr6: 107,868,737-108,177,185 RNU6-437P, RPL3P7, 7 more genes
    nsv6636921copy number variation1nstd102humanUncertain significance GRCh37 chr6: 108,195,840-108,498,389 , GRCh38.p12 chr6: 107,874,636-108,177,185 MTHFD2P3, RPL3P7, 7 more genes
    nsv6630706copy number variation1nstd224human GRCh37 chr6: 108,214,694-108,395,722 , GRCh38.p12 chr6: 107,893,490-108,074,518 SEC63, OSTM1, 5 more genes
    nsv6617952copy number variation1nstd223human GRCh38 chr6: 108,067,637-108,069,526 , GRCh37.p13 chr6: 108,388,841-108,390,730 OSTM1
    nsv6610764copy number variation1nstd223human GRCh38 chr6: 108,046,157-108,046,574 , GRCh37.p13 chr6: 108,367,361-108,367,778 OSTM1
    nsv6604373copy number variation1nstd223human GRCh38 chr6: 108,074,201-108,075,500 , GRCh37.p13 chr6: 108,395,405-108,396,704 OSTM1
    nsv6561067inversion1nstd223human GRCh38 chr6: 108,072,415-108,072,844 , GRCh37.p13 chr6: 108,393,619-108,394,048 OSTM1
    nsv6559708inversion1nstd223human GRCh38 chr6: 108,070,327-108,070,950 , GRCh37.p13 chr6: 108,391,531-108,392,154 OSTM1
    nsv6313858copy number variation1nstd102humanPathogenic GRCh37 chr6: 92,054,891-118,329,651 , GRCh38.p12 chr6: 91,345,173-118,008,488 RN7SL509P, LAMA4, 311 more genes
    nsv5716960mobile element insertion1nstd211human GRCh38 chr6: 108,062,190-108,062,190 , GRCh37.p13 chr6: 108,383,394-108,383,394 OSTM1
    nsv5685280mobile element insertion1nstd211human GRCh38 chr6: 108,061,936-108,061,936 , GRCh37.p13 chr6: 108,383,140-108,383,140 OSTM1
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