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Items: 1 to 20 of 212

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148117copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,611,360-89,264,122 , GRCh38.p12 chr10: 79,851,604-87,504,365 ANXA11, FAM245A, 115 more genes
    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
    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
    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
    nsv7067649inversion1nstd229human GRCh38 chr10: 87,018,739-87,020,260 , GRCh37.p13 chr10: 88,778,496-88,780,017 FAM25A
    nsv7065381inversion1nstd229human GRCh38 chr10: 83,674,811-92,070,275 , GRCh37.p13 chr10: 85,434,567-93,830,032 LINC01520, RPS27P1, 158 more genes
    nsv7058867inversion1nstd229human GRCh38 chr10: 86,821,907-87,259,713 , GRCh37.p13 chr10: 88,581,664-89,019,470 BMS1P3, LOC105378410, 14 more genes
    nsv6889467copy number variation1nstd229human GRCh38 chr10: 87,023,450-87,023,509 , GRCh37.p13 chr10: 88,783,207-88,783,266 FAM25A
    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
    nsv6637457copy number variation1nstd102humanUncertain significance GRCh37 chr10: 88,578,693-88,863,385 , GRCh38.p12 chr10: 86,818,936-87,103,628 MMRN2, RNU6-529P, 10 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
    nsv6620851copy number variation1nstd224human GRCh37 chr10: 88,227,155-88,946,889 , GRCh38.p12 chr10: 86,467,398-87,187,132 BMPR1A, GLUD1, 20 more genes
    nsv6585055inversion1nstd223human GRCh38 chr10: 79,754,380-87,461,415 , GRCh37.p13 chr10: 81,514,136-89,221,172 DYDC2, LOC105378394, 114 more genes
    nsv6453102copy number variation1nstd223human GRCh38 chr10: 87,025,156-87,026,000 , GRCh37.p13 chr10: 88,784,913-88,785,757 FAM25A
    nsv6452820copy number variation1nstd223human GRCh38 chr10: 87,000,010-87,045,517 , GRCh37.p13 chr10: 88,759,767-88,805,274 FAM25A, BMS1P3, 2 more genes
    nsv6451688copy number variation1nstd223human GRCh38 chr10: 87,019,399-87,067,528 , GRCh37.p13 chr10: 88,779,156-88,827,285 GLUD1, RNU6-529P, 1 more genes
    nsv6315478copy number variation1nstd102humanPathogenic GRCh37 chr10: 81,630,468-88,980,961 , GRCh38.p12 chr10: 79,870,712-87,221,204 RNU1-19P, LOC107984187, 102 more genes
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