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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054442inversion1nstd229human GRCh38 chr3: 87,091,910-87,091,965 , GRCh37.p13 chr3: 87,141,060-87,141,115 LINC00506
    nsv7039090inversion1nstd229human GRCh38 chr3: 87,032,755-87,095,270 , GRCh37.p13 chr3: 87,081,905-87,144,420 LINC00506, LOC285232, 1 more genes
    nsv6717759copy number variation1nstd229human GRCh38 chr3: 87,126,097-87,133,650 , GRCh37.p13 chr3: 87,175,247-87,182,800 LINC00506
    nsv6717353copy number variation1nstd229human GRCh38 chr3: 87,128,045-87,130,732 , GRCh37.p13 chr3: 87,177,195-87,179,882 LINC00506
    nsv6716022copy number variation1nstd229human GRCh38 chr3: 87,127,001-87,134,200 , GRCh37.p13 chr3: 87,176,151-87,183,350 LINC00506
    nsv6715189copy number variation1nstd229human GRCh38 chr3: 87,133,405-87,181,795 , GRCh37.p13 chr3: 87,182,555-87,230,945 LINC00506
    nsv6714029copy number variation1nstd229human GRCh38 chr3: 87,119,695-87,119,864 , GRCh37.p13 chr3: 87,168,845-87,169,014 LINC00506
    nsv6711162copy number variation1nstd229human GRCh38 chr3: 87,107,943-87,111,755 , GRCh37.p13 chr3: 87,157,093-87,160,905 LINC00506
    nsv6710365copy number variation1nstd229human GRCh38 chr3: 87,093,653-87,093,733 , GRCh37.p13 chr3: 87,142,803-87,142,883 LINC00506
    nsv6703689copy number variation1nstd229human GRCh38 chr3: 87,145,701-87,160,500 , GRCh37.p13 chr3: 87,194,851-87,209,650 LINC00506
    nsv6701950copy number variation1nstd229human GRCh38 chr3: 87,147,527-87,156,191 , GRCh37.p13 chr3: 87,196,677-87,205,341 LINC00506
    nsv6636809copy number variation1nstd102humanUncertain significance GRCh37 chr3: 86,841,601-87,862,816 , GRCh38.p12 chr3: 86,792,451-87,813,666 CHMP2B, POU1F1, 12 more genes
    nsv6373348copy number variation1nstd223human GRCh38 chr3: 87,134,001-87,135,000 , GRCh37.p13 chr3: 87,183,151-87,184,150 LINC00506
    nsv6373112copy number variation1nstd223human GRCh38 chr3: 87,102,901-87,104,700 , GRCh37.p13 chr3: 87,152,051-87,153,850 LINC00506
    nsv6368410copy number variation1nstd223human GRCh38 chr3: 87,116,167-87,116,571 , GRCh37.p13 chr3: 87,165,317-87,165,721 LINC00506
    nsv6368234copy number variation1nstd223human GRCh38 chr3: 87,151,901-87,156,800 , GRCh37.p13 chr3: 87,201,051-87,205,950 LINC00506
    nsv6359411copy number variation1nstd223human GRCh38 chr3: 87,123,201-87,127,400 , GRCh37.p13 chr3: 87,172,351-87,176,550 LINC00506
    nsv6357884copy number variation1nstd223human GRCh38 chr3: 87,080,886-87,091,513 , GRCh37.p13 chr3: 87,130,036-87,140,663 LINC00506
    nsv6314751copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 72,488,757-99,614,758 , GRCh38.p12 chr3: 72,439,606-99,895,914 AKR1B1P2, COL8A1, 231 more genes
    nsv6290743copy number variation1nstd102humanUncertain significance GRCh37 chr3: 87,158,116-87,306,158 , GRCh38.p12 chr3: 87,108,966-87,257,008 MIR4795, LINC00506, 1 more genes
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