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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974534inversion1nstd209human GRCh38 chr17: 15,750,079-18,634,890 , GRCh37.p13 chr17: 15,653,393-18,538,203 , ADORA2B, 119 more genes
    nsv5945891copy number variation1nstd209human GRCh38 chr17: 15,750,946-16,668,217 , GRCh37.p13 chr17: 15,654,260-16,571,531 ADORA2B, MIR1288, 34 more genes
    nsv5943631copy number variation1nstd209human GRCh38 chr17: 15,758,933-16,863,323 , GRCh37.p13 chr17: 15,662,247-16,766,637 , MIR1288, 50 more genes
    nsv5940764copy number variation1nstd209human GRCh38 chr17: 15,758,291-16,862,696 , GRCh37.p13 chr17: 15,661,605-16,766,010 , ZSWIM5P1, 50 more genes
    nsv5557306sequence alteration1nstd206human GRCh38 chr17: 16,372,615-16,575,020 , GRCh37.p13 chr17: 16,275,929-16,478,334 LOC105371554, SNORD49A, 8 more genes
    nsv5527117copy number variation1nstd206human GRCh38 chr17: 16,379,548-16,380,356 , GRCh37.p13 chr17: 16,282,862-16,283,670 UBB
    nsv5304853copy number variation1nstd204human GRCh38.p13 chr17: 16,376,946-16,380,110 , GRCh37.p13 chr17: 16,280,260-16,283,424 UBB
    nsv5292764copy number variation1nstd204human GRCh38.p13 chr17: 16,376,900-16,379,849 , GRCh37.p13 chr17: 16,280,214-16,283,163 UBB
    nsv5026068copy number variation1nstd200human GRCh38 chr17: 16,377,610-16,380,176 , GRCh37.p13 chr17: 16,280,924-16,283,490 UBB
    nsv5026064copy number variation1nstd200human GRCh38 chr17: 16,355,197-16,380,173 , GRCh37.p13 chr17: 16,258,511-16,283,487 UBB
    nsv4858211copy number variation1nstd200human GRCh37 chr17: 16,280,267-16,283,417 , GRCh38.p12 chr17: 16,376,953-16,380,103 UBB
    nsv4858206copy number variation1nstd200human GRCh37 chr17: 16,258,511-16,283,487 , GRCh38.p12 chr17: 16,355,197-16,380,173 UBB
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729936copy number variation1nstd102humanUncertain significance GRCh37 chr17: 15,688,146-16,756,345 , GRCh38.p12 chr17: 15,784,832-16,853,031 ZNF624, RNU6-862P, 45 more genes
    nsv4729930copy number variation1nstd102humanUncertain significance GRCh37 chr17: 15,688,146-16,769,801 , GRCh38.p12 chr17: 15,784,832-16,866,487 LOC105371557, SPECC1P1, 45 more genes
    nsv4729738copy number variation1nstd102humanPathogenic GRCh37 chr17: 15,810,015-18,537,436 , GRCh38.p12 chr17: 15,906,701-18,634,123 UPF3AP1, ADORA2B, 109 more genes
    nsv4681821copy number variation1nstd102humanUncertain significance GRCh37 chr17: 16,120,521-16,875,409 , GRCh38.p12 chr17: 16,217,207-16,972,095 SRP68P1, LOC105371552, 33 more genes
    nsv4675813copy number variation1nstd102humanUncertain significance GRCh37 chr17: 15,722,839-16,763,698 , GRCh38.p12 chr17: 15,819,525-16,860,384 CCDC144A, CENPV, 42 more genes
    nsv4675003copy number variation1nstd102humanPathogenic GRCh37 chr17: 15,632,431-18,726,389 , GRCh38.p12 chr17: 15,729,117-18,823,076 LLGL1, LOC107985051, 127 more genes
    nsv4674993copy number variation1nstd102humanUncertain significance GRCh37 chr17: 15,730,101-16,591,260 , GRCh38.p12 chr17: 15,826,787-16,687,946 NEK4P2, RNASEH1P2, 28 more genes
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