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Items: 1 to 20 of 224

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099255copy number variation1nstd231human GRCh38.p12 chr1: 192,358,641-201,911,882 , GRCh37 chr1: 192,327,771-201,881,010 CACNA1S, CSRP1, 120 more genes
    nsv7095955copy number variation1nstd102humanUncertain significance GRCh37 chr1: 200,522,516-206,945,780 , GRCh38.p12 chr1: 200,553,388-206,772,435 ELF3, MAPKAPK2, 189 more genes
    nsv7095569copy number variation2nstd102humanUncertain significance GRCh37 chr1: 200,522,516-208,391,267 , GRCh38.p12 chr1: 200,553,388-208,217,922 TRK-TTT8-1, ADIPOR1, 228 more genes
    nsv7049604inversion1nstd229human GRCh38 chr1: 200,813,229-200,922,460 , GRCh37.p13 chr1: 200,782,357-200,891,588 GPR25, CAMSAP2, 2 more genes
    nsv7048044inversion1nstd229human GRCh38 chr1: 200,722,696-202,712,068 , GRCh37.p13 chr1: 200,691,824-202,681,196 ARL8A, KIF21B, 52 more genes
    nsv7047837inversion1nstd229human GRCh38 chr1: 200,858,159-200,933,533 , GRCh37.p13 chr1: 200,827,287-200,902,661 RNU6-704P, RPL34P6, 4 more genes
    nsv6676308copy number variation1nstd229human GRCh38 chr1: 200,829,910-201,044,780 , GRCh37.p13 chr1: 200,799,038-201,013,908 CAMSAP2, KIF21B, 7 more genes
    nsv6673647copy number variation1nstd229human GRCh38 chr1: 200,873,101-201,555,700 , GRCh37.p13 chr1: 200,842,229-201,524,828 GPR25, PHLDA3, 18 more genes
    nsv6671887copy number variation1nstd229human GRCh38 chr1: 200,816,942-200,932,927 , GRCh37.p13 chr1: 200,786,070-200,902,055 RPL34P6, CAMSAP2, 4 more genes
    nsv6670757copy number variation1nstd229human GRCh38 chr1: 200,819,311-200,907,137 , GRCh37.p13 chr1: 200,788,439-200,876,265 CAMSAP2, GPR25, 2 more genes
    nsv6669227copy number variation1nstd229human GRCh38 chr1: 200,818,368-201,023,680 , GRCh37.p13 chr1: 200,787,496-200,992,808 RPL34P6, RNU6-704P, 6 more genes
    nsv6667757copy number variation1nstd229human GRCh38 chr1: 200,891,919-200,895,493 , GRCh37.p13 chr1: 200,861,047-200,864,621 INAVA
    nsv6665429copy number variation1nstd229human GRCh38 chr1: 200,816,938-200,949,316 , GRCh37.p13 chr1: 200,786,066-200,918,444 RPL34P6, INAVA, 4 more genes
    nsv6664810copy number variation1nstd229human GRCh38 chr1: 200,816,944-200,924,647 , GRCh37.p13 chr1: 200,786,072-200,893,775 GPR25, INAVA, 2 more genes
    nsv6664216copy number variation1nstd229human GRCh38 chr1: 200,890,639-200,897,432 , GRCh37.p13 chr1: 200,859,767-200,866,560 INAVA
    nsv6661464copy number variation1nstd229human GRCh38 chr1: 200,886,562-200,893,637 , GRCh37.p13 chr1: 200,855,690-200,862,765 INAVA
    nsv6659212copy number variation1nstd229human GRCh38 chr1: 200,816,945-200,890,797 , GRCh37.p13 chr1: 200,786,073-200,859,925 GPR25, CAMSAP2, 2 more genes
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6636485copy number variation1nstd102humanUncertain significance GRCh37 chr1: 200,795,738-201,013,947 , GRCh38.p12 chr1: 200,826,610-201,044,819 INAVA, LOC101929305, 7 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
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