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Items: 1 to 20 of 204

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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
    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
    nsv6884177copy number variation1nstd229human GRCh38 chr10: 86,966,284-86,980,821 , GRCh37.p13 chr10: 88,726,041-88,740,578 ADIRF, AGAP11, 1 more genes
    nsv6883597copy number variation1nstd229human GRCh38 chr10: 86,967,176-86,967,201 , GRCh37.p13 chr10: 88,726,933-88,726,958 ADIRF, MMRN2
    nsv6881306copy number variation1nstd229human GRCh38 chr10: 86,960,101-86,968,300 , GRCh37.p13 chr10: 88,719,858-88,728,057 ADIRF, SNCG, 1 more genes
    nsv6881038copy number variation1nstd229human GRCh38 chr10: 86,969,043-86,974,815 , GRCh37.p13 chr10: 88,728,800-88,734,572 ADIRF, MMRN2, 1 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
    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
    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
    nsv6291365copy number variation1nstd102humanUncertain significance GRCh37 chr10: 88,639,431-88,973,306 , GRCh38.p12 chr10: 86,879,674-87,213,549 BMS1P3, LOC105378410, 11 more genes
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