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Items: 1 to 20 of 317

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7062023inversion1nstd229human GRCh38 chr10: 70,360,585-70,360,912 , GRCh37.p13 chr10: 72,120,341-72,120,668 LRRC20
    nsv6897196copy number variation1nstd229human GRCh38 chr10: 70,322,048-70,322,110 , GRCh37.p13 chr10: 72,081,804-72,081,866 LRRC20
    nsv6895758copy number variation1nstd229human GRCh38 chr10: 70,361,978-70,364,094 , GRCh37.p13 chr10: 72,121,734-72,123,850 LRRC20
    nsv6894015copy number variation1nstd229human GRCh38 chr10: 70,367,088-70,369,829 , GRCh37.p13 chr10: 72,126,844-72,129,585 LRRC20
    nsv6887594copy number variation1nstd229human GRCh38 chr10: 70,366,002-70,377,032 , GRCh37.p13 chr10: 72,125,758-72,136,788 LRRC20
    nsv6885769copy number variation1nstd229human GRCh38 chr10: 70,325,501-70,328,200 , GRCh37.p13 chr10: 72,085,257-72,087,956 LRRC20
    nsv6881191copy number variation1nstd229human GRCh38 chr10: 70,335,382-70,335,540 , GRCh37.p13 chr10: 72,095,138-72,095,296 LRRC20
    nsv6879452copy number variation1nstd229human GRCh38 chr10: 70,332,301-70,348,100 , GRCh37.p13 chr10: 72,092,057-72,107,856 LRRC20
    nsv6620675copy number variation1nstd224human GRCh37 chr10: 72,012,813-73,062,048 , GRCh38.p12 chr10: 70,253,057-71,302,291 ADAMTS14, TBATA, 17 more genes
    nsv6620606copy number variation1nstd224human GRCh37 chr10: 72,109,893-72,996,234 , GRCh38.p12 chr10: 70,350,137-71,236,477 NODAL, PCBD1, 15 more genes
    nsv6445680copy number variation1nstd223human GRCh38 chr10: 70,240,835-70,305,787 , GRCh37.p13 chr10: 72,000,591-72,065,543 LRRC20, NPFFR1
    nsv6444872copy number variation1nstd223human GRCh38 chr10: 70,293,423-70,921,060 , GRCh37.p13 chr10: 72,053,179-72,680,817 PALD1, YY1P1, 10 more genes
    nsv6314185copy number variation1nstd102humanPathogenic GRCh37 chr10: 68,735,254-78,885,714 , GRCh38.p12 chr10: 66,975,496-77,125,956 SLC25A16, CTNNA3, 204 more genes
    nsv6291213copy number variation1nstd102humanUncertain significance GRCh37 chr10: 71,754,361-72,399,690 , GRCh38.p12 chr10: 69,994,605-70,639,934 MACROH2A2, CEP57L1P1, 14 more genes
    nsv6281317insertion3nstd214human GRCh38 chr10: 70,367,962-70,367,962 , GRCh37.p13 chr10: 72,127,718-72,127,718 LRRC20
    nsv6210356insertion1nstd214human GRCh38 chr10: 70,367,968-70,367,968 , GRCh37.p13 chr10: 72,127,724-72,127,724 LRRC20
    nsv6131888copy number variation1nstd213human GRCh37 chr10: 71,890,000-72,730,001 , GRCh38.p12 chr10: 70,130,244-70,970,244 NPFFR1, TBATA, 18 more genes
    nsv6083167insertion1nstd212human GRCh38 chr10: 70,367,958-70,367,958 , GRCh37.p13 chr10: 72,127,714-72,127,714 LRRC20
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