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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6728951copy number variation1nstd229human GRCh38 chr3: 146,840,344-146,931,116 , GRCh37.p13 chr3: 146,558,131-146,648,903 LINC02010
    nsv6722569copy number variation1nstd229human GRCh38 chr3: 146,860,054-146,965,411 , GRCh37.p13 chr3: 146,577,841-146,683,198 LINC02010
    nsv6722012copy number variation1nstd229human GRCh38 chr3: 146,918,301-146,921,300 , GRCh37.p13 chr3: 146,636,088-146,639,087 LINC02010
    nsv6718514copy number variation1nstd229human GRCh38 chr3: 146,921,573-146,925,370 , GRCh37.p13 chr3: 146,639,360-146,643,157 LINC02010
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6628652copy number variation1nstd224human GRCh37 chr3: 146,396,006-146,764,697 , GRCh38.p12 chr3: 146,678,219-147,046,910 RNU6-505P, LOC112268449, 1 more genes
    nsv6628457copy number variation1nstd224human GRCh37 chr3: 146,414,212-146,764,697 , GRCh38.p12 chr3: 146,696,425-147,046,910 LINC02010, RNU6-505P, 1 more genes
    nsv6628280copy number variation1nstd224human GRCh37 chr3: 146,584,464-146,666,094 , GRCh38.p12 chr3: 146,866,677-146,948,307 LINC02010
    nsv6562831inversion1nstd223human GRCh38 chr3: 142,555,219-148,451,915 , GRCh37.p13 chr3: 142,274,061-148,169,702 LOC102724145, PLS1, 60 more genes
    nsv6374176copy number variation1nstd223human GRCh38 chr3: 146,673,629-147,074,789 , GRCh37.p13 chr3: 146,391,416-146,792,576 LOC112268449, LINC02010, 1 more genes
    nsv6369455copy number variation1nstd223human GRCh38 chr3: 146,860,051-146,965,410 , GRCh37.p13 chr3: 146,577,838-146,683,197 LINC02010
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6290273copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295 LINC02066, TM4SF1-AS1, 206 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv6134994copy number variation1nstd213human GRCh37 chr3: 139,490,000-150,360,001 , GRCh38.p12 chr3: 139,771,158-150,642,214 , ATP1B3, 147 more genes
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5301803copy number variation1nstd204human GRCh38.p13 chr3: 145,088,231-147,513,312 , GRCh37.p13 chr3: 144,806,005-147,231,099 LINC02010, ZIC1, 21 more genes
    nsv5034922inversion1nstd200human GRCh38 chr3: 137,979,992-148,451,901 , GRCh37.p13 chr3: 137,698,834-148,169,688 , LOC105374148, 132 more genes
    nsv4873274inversion1nstd200human GRCh37 chr3: 137,698,834-148,169,688 , GRCh38.p12 chr3: 137,979,992-148,451,901 , PLSCR5, 132 more genes
    nsv4791387copy number variation1nstd200human GRCh37 chr3: 144,806,010-147,231,090 , GRCh38.p12 chr3: 145,088,236-147,513,303 RPL21P71, PLSCR2, 21 more genes
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