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Items: 1 to 20 of 183

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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
    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
    nsv6890084copy number variation1nstd229human GRCh38 chr10: 88,706,783-88,838,566 , GRCh37.p13 chr10: 90,466,540-90,598,323 LIPM, ANKRD22, 4 more genes
    nsv6886584copy number variation1nstd229human GRCh38 chr10: 88,822,658-88,828,311 , GRCh37.p13 chr10: 90,582,415-90,588,068 ANKRD22
    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
    nsv6879237copy number variation1nstd229human GRCh38 chr10: 88,807,622-88,836,969 , GRCh37.p13 chr10: 90,567,379-90,596,726 ANKRD22, LIPM
    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
    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
    nsv6620856copy number variation2nstd224human GRCh37 chr10: 90,477,590-90,596,859 , GRCh38.p12 chr10: 88,717,833-88,837,102 ANKRD22, LIPM, 4 more genes
    nsv6441034copy number variation1nstd223human GRCh38 chr10: 88,827,301-88,829,200 , GRCh37.p13 chr10: 90,587,058-90,588,957 ANKRD22
    nsv6440252copy number variation1nstd223human GRCh38 chr10: 88,706,783-88,838,563 , GRCh37.p13 chr10: 90,466,540-90,598,320 LIPN, ANKRD22, 4 more genes
    nsv6208573insertion1nstd214human GRCh38 chr10: 88,832,453-88,832,453 , GRCh37.p13 chr10: 90,592,210-90,592,210 ANKRD22
    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
    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
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