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Items: 1 to 20 of 113

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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
    nsv7093656copy number variation1nstd102humanUncertain significance GRCh37 chr10: 90,697,798-90,767,614 , GRCh38.p12 chr10: 88,938,041-89,007,857 ACTA2, FAS-AS1, 2 more genes
    nsv7074617inversion1nstd229human GRCh38 chr10: 86,025,751-89,446,782 , GRCh37.p13 chr10: 87,785,508-91,206,539 GRID1, LDB3, 83 more genes
    nsv7073898inversion1nstd229human GRCh38 chr10: 85,457,267-89,078,986 , GRCh37.p13 chr10: 87,217,024-90,838,743 LOC112268064, LOC105378416, 74 more genes
    nsv7073007inversion1nstd229human GRCh38 chr10: 83,678,437-92,070,274 , GRCh37.p13 chr10: 85,438,193-93,830,031 PPP1R3C, LOC105378415, 157 more genes
    nsv7065381inversion1nstd229human GRCh38 chr10: 83,674,811-92,070,275 , GRCh37.p13 chr10: 85,434,567-93,830,032 LINC01520, RPS27P1, 158 more genes
    nsv6893510copy number variation1nstd229human GRCh38 chr10: 88,357,217-89,008,456 , GRCh37.p13 chr10: 90,116,974-90,768,213 PTCD2P2, ACTA2, 16 more genes
    nsv6883259copy number variation1nstd229human GRCh38 chr10: 88,909,886-89,428,064 , GRCh37.p13 chr10: 90,669,643-91,187,821 IFIT2, STAMBPL1, 18 more genes
    nsv6881199copy number variation1nstd229human GRCh38 chr10: 88,487,671-89,149,734 , GRCh37.p13 chr10: 90,247,428-90,909,491 PTCD2P2, LOC100289238, 18 more genes
    nsv6637868copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,823,147-96,056,941 , GRCh38.p12 chr10: 88,063,390-94,297,184 RPS27P1, RNLS, 118 more genes
    nsv6637707copy number variation1nstd102humanUncertain significance GRCh37 chr10: 90,672,265-91,165,763 , GRCh38.p12 chr10: 88,912,508-89,406,006 IFIT1, IFIT3, 16 more genes
    nsv6637542copy number variation1nstd102humanPathogenic GRCh37 chr10: 82,595,472-93,542,416 , GRCh38.p12 chr10: 80,835,716-91,782,659 IFIT6P, HECTD2, 166 more genes
    nsv6634458copy number variation1nstd102humanPathogenic GRCh37 chr10: 83,533,660-91,913,077 , GRCh38.p12 chr10: 81,773,904-90,153,320 IFIT5, IFIT1, 140 more genes
    nsv6450726copy number variation1nstd223human GRCh38 chr10: 88,936,714-89,008,323 , GRCh37.p13 chr10: 90,696,471-90,768,080 ACTA2-AS1, FAS, 2 more genes
    nsv6447142copy number variation1nstd223human GRCh38 chr10: 88,987,901-88,993,600 , GRCh37.p13 chr10: 90,747,658-90,753,357 FAS-AS1, FAS, 1 more genes
    nsv6309171copy number variation1nstd102humanUncertain significance GRCh37 chr10: 90,694,970-91,007,415 , GRCh38.p12 chr10: 88,935,213-89,247,658 FAS-AS1, LOC100289238, 8 more genes
    nsv6309015copy number variation1nstd102humanPathogenic GRCh37 chr10: 90,749,963-90,750,683 , GRCh38.p12 chr10: 88,990,206-88,990,926 ACTA2, FAS, 1 more genes
    nsv6247360mobile element insertion1nstd215human GRCh38 chr10: 88,992,310-88,992,310 , GRCh37.p13 chr10: 90,752,067-90,752,067 FAS, FAS-AS1
    nsv6131982copy number variation1nstd213human GRCh37 chr10: 90,510,000-91,010,001 , GRCh38.p12 chr10: 88,750,243-89,250,244 ACTA2, FAS, 15 more genes
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