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Items: 1 to 20 of 139

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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
    nsv7137134copy number variation1nstd102humannot provided GRCh37 chr10: 89,685,057-89,721,049 , GRCh38.p12 chr10|NW_013171807.1: 141,092-177,081 , GRCh38.p12 chr10: 87,925,300-87,961,292 PTEN, RPL11P3
    nsv7093895copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,428,449-89,725,229 , GRCh38.p12 chr10: 86,668,692-87,965,472 LOC105378410, PAPSS2, 33 more genes
    nsv7093741copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,514,444-90,537,999 , GRCh38.p12 chr10: 87,754,687-88,778,242 LIPK, LOC105378416, 18 more genes
    nsv7093655copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,621,800-89,725,321 , GRCh38.p12 chr10: 87,862,043-87,965,564 , GRCh38.p12 chr10|NW_013171807.1: 77,867-181,353 KLLN, PTEN, 1 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
    nsv7070109inversion1nstd229human GRCh38 chr10: 87,536,871-87,971,064 , GRCh37.p13 chr10: 89,296,628-89,730,821 PAPSS2, PTEN, 8 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
    nsv6893211copy number variation1nstd229human GRCh38 chr10: 87,944,448-87,944,587 , GRCh37.p13 chr10: 89,704,205-89,704,344 RPL11P3, PTEN
    nsv6887740copy number variation1nstd229human GRCh38 chr10: 87,934,973-87,947,752 , GRCh37.p13 chr10: 89,694,730-89,707,509 RPL11P3, PTEN
    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
    nsv6315464copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,698,323-90,252,519 , GRCh38.p12 chr10: 87,938,566-88,492,762 PTEN, RNLS, 7 more genes
    nsv6309170copy number variation1nstd102humanPathogenic GRCh37 chr10: 89,622,928-89,725,229 , GRCh38.p12 chr10: 87,863,171-87,965,472 , GRCh38.p12 chr10|NW_013171807.1: 78,995-181,261 KLLN, PTEN, 1 more genes
    nsv6131981copy number variation1nstd213human GRCh37 chr10: 86,230,000-90,870,001 , GRCh38.p12 chr10: 84,470,244-89,110,244 ACTA2, FAS, 84 more genes
    nsv6131980copy number variation2nstd213human GRCh37 chr10: 86,230,000-90,860,001 , GRCh38.p12 chr10: 84,470,244-89,100,244 ACTA2, FAS, 84 more genes
    nsv6131817copy number variation1nstd213human GRCh37 chr10: 89,670,000-90,510,001 , GRCh38.p12 chr10: 87,910,243-88,750,244 PTEN, LIPF, 13 more genes
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