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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7044513inversion1nstd229human GRCh38 chr3: 131,210,998-138,882,695 , GRCh37.p13 chr3: 130,929,842-138,601,537 HSPA8P9, RNU6-1174P, 114 more genes
    nsv6736272copy number variation1nstd229human GRCh38 chr3: 131,379,301-131,388,200 , GRCh37.p13 chr3: 131,098,145-131,107,044 NUDT16-DT, NUDT16
    nsv6734201copy number variation1nstd229human GRCh38 chr3: 131,271,919-131,477,783 , GRCh37.p13 chr3: 130,990,763-131,196,627 LOC105374110, NUDT16, 6 more genes
    nsv6732555copy number variation1nstd229human GRCh38 chr3: 131,347,351-131,348,086 , GRCh37.p13 chr3: 131,066,195-131,066,930 NUDT16-DT, NEK11
    nsv6731892copy number variation1nstd229human GRCh38 chr3: 131,379,137-131,379,218 , GRCh37.p13 chr3: 131,097,981-131,098,062 NUDT16-DT
    nsv6728537copy number variation1nstd229human GRCh38 chr3: 131,361,901-131,382,200 , GRCh37.p13 chr3: 131,080,745-131,101,044 NUDT16, NUDT16L2P, 1 more genes
    nsv6721146copy number variation1nstd229human GRCh38 chr3: 131,323,275-131,323,319 , GRCh37.p13 chr3: 131,042,119-131,042,163 NEK11, NUDT16-DT
    nsv6720515copy number variation1nstd229human GRCh38 chr3: 131,315,650-131,340,465 , GRCh37.p13 chr3: 131,034,494-131,059,309 NUDT16-DT, NEK11
    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
    nsv6628642copy number variation1nstd224human GRCh37 chr3: 131,041,928-131,471,873 , GRCh38.p12 chr3: 131,323,084-131,753,029 NUDT16-DT, MRPL3, 9 more genes
    nsv6374525copy number variation1nstd223human GRCh38 chr3: 131,362,348-131,382,222 , GRCh37.p13 chr3: 131,081,192-131,101,066 NUDT16, NUDT16-DT, 1 more genes
    nsv6368230copy number variation1nstd223human GRCh38 chr3: 131,361,340-131,381,055 , GRCh37.p13 chr3: 131,080,184-131,099,899 NUDT16, NUDT16-DT, 1 more genes
    nsv6364624copy number variation1nstd223human GRCh38 chr3: 131,345,541-131,346,604 , GRCh37.p13 chr3: 131,064,385-131,065,448 NEK11, NUDT16-DT
    nsv6311770copy number variation1nstd102humanPathogenic GRCh37 chr3: 120,365,818-133,465,047 , GRCh38.p12 chr3: 120,646,971-133,746,203 HNRNPA1P23, MIX23, 278 more genes
    nsv6277219insertion2nstd214human GRCh38 chr3: 131,357,275-131,357,275 , GRCh37.p13 chr3: 131,076,119-131,076,119 NUDT16-DT
    nsv6254679mobile element insertion1nstd215human GRCh38 chr3: 131,338,313-131,338,313 , GRCh37.p13 chr3: 131,057,157-131,057,157 NEK11, NUDT16-DT
    nsv6219629insertion3nstd214human GRCh38 chr3: 131,357,263-131,357,263 , GRCh37.p13 chr3: 131,076,107-131,076,107 NUDT16-DT
    nsv6165005copy number variation1nstd214human GRCh38 chr3: 131,379,134-131,379,217 , GRCh37.p13 chr3: 131,097,978-131,098,061 NUDT16-DT
    nsv6139579copy number variation1nstd206human GRCh38 chr3: 131,323,574-131,341,574 , GRCh37.p13 chr3: 131,042,418-131,060,418 NEK11, NUDT16-DT
    nsv6134575copy number variation1nstd213human GRCh37 chr3: 116,870,000-132,100,001 , GRCh38.p12 chr3: 117,151,153-132,381,157 ACP3, ADCY5, 308 more genes
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