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Items: 1 to 20 of 443

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5344555translocation1nstd200human GRCh37 chr10: 45,707,357-45,707,357 , GRCh37 chr10: 45,707,280-45,707,280 , GRCh38.p12 chr10|NW_003315935.1: 36,677-36,677 , GRCh38.p12 chr10|NW_003315935.1: 36,600-36,600 , GRCh38.p12 chr10: 45,211,832-45,211,832 , GRCh38.p12 chr10: 45,211,909-45,211,909 LOC105378283
    nsv4847682copy number variation1nstd200human GRCh37 chr10: 45,842,209-45,844,018 , GRCh38.p12 chr10: 45,346,761-45,348,570 , GRCh38.p12 chr10|NW_003315935.1: 187,551-189,400 0
    nsv4844155copy number variation1nstd200human GRCh37 chr10: 45,893,075-45,893,197 , GRCh38.p12 chr10: 45,397,627-45,397,749 , GRCh38.p12 chr10|NW_003315935.1: 238,458-238,580 ALOX5
    nsv4840949copy number variation1nstd200human GRCh37 chr10: 45,687,115-45,706,568 , GRCh38.p12 chr10: 45,191,667-45,211,120 , GRCh38.p12 chr10|NW_003315935.1: 16,435-35,888 LOC105378283
    nsv4839748copy number variation1nstd200human GRCh37 chr10: 45,762,469-45,763,889 , GRCh38.p12 chr10|NW_003315935.1: 91,789-93,209 , GRCh38.p12 chr10: 45,267,021-45,268,441 0
    nsv4839095copy number variation1nstd200human GRCh37 chr10: 45,766,949-45,772,348 , GRCh38.p12 chr10: 45,271,501-45,276,900 , GRCh38.p12 chr10|NW_003315935.1: 96,269-101,668 0
    nsv4837959copy number variation1nstd200human GRCh37 chr10: 45,692,419-45,693,756 , GRCh38.p12 chr10: 45,196,971-45,198,308 , GRCh38.p12 chr10|NW_003315935.1: 21,739-23,076 LOC105378283
    nsv4835853copy number variation1nstd200human GRCh37 chr10: 45,758,055-45,771,039 , GRCh38.p12 chr10: 45,262,607-45,275,591 , GRCh38.p12 chr10|NW_003315935.1: 87,375-100,359 0
    nsv4834121copy number variation1nstd200human GRCh37 chr10: 45,728,770-45,731,642 , GRCh38.p12 chr10: 45,233,322-45,236,194 , GRCh38.p12 chr10|NW_003315935.1: 58,090-60,962 CUBNP2
    nsv4829641copy number variation1nstd200human GRCh37 chr10: 45,815,099-45,820,072 , GRCh38.p12 chr10: 45,319,651-45,324,624 , GRCh38.p12 chr10|NW_003315935.1: 144,419-149,395 0
    nsv4829618copy number variation1nstd200human GRCh37 chr10: 45,843,346-45,843,931 , GRCh38.p12 chr10: 45,347,898-45,348,483 , GRCh38.p12 chr10|NW_003315935.1: 188,728-189,313 0
    nsv4769357copy number variation1nstd102humanUncertain significance GRCh37 chr10: 45,758,657-46,021,583 , GRCh38.p12 chr10|NW_003315935.1: 87,977-309,802 , GRCh38.p12 chr10: 45,263,209-45,526,135 ALOX5, OR13A1, 3 more genes
    nsv4715088copy number variation1nstd195human GRCh37 chr10: 45,741,701-45,750,001 , GRCh38.p12 chr10: 45,246,253-45,254,553 , GRCh38.p12 chr10|NW_003315935.1: 71,021-79,321 CUBNP2
    nsv4713255copy number variation1nstd195human GRCh37 chr10: 45,728,767-45,728,768 , GRCh38.p12 chr10: 45,233,319-45,233,320 , GRCh38.p12 chr10|NW_003315935.1: 58,087-58,088 CUBNP2
    nsv4671670copy number variation1nstd186human GRCh37 chr10: 45,728,767-45,731,642 , GRCh38.p12 chr10: 45,233,319-45,236,194 , GRCh38.p12 chr10|NW_003315935.1: 58,087-60,962 CUBNP2
    nsv4671154copy number variation1nstd186human GRCh37 chr10: 45,752,214-45,752,870 , GRCh38.p12 chr10|NW_003315935.1: 81,534-82,190 , GRCh38.p12 chr10: 45,256,766-45,257,422 OR6D1P
    nsv4669405copy number variation1nstd186human GRCh37 chr10: 45,728,819-45,731,678 , GRCh38.p12 chr10: 45,233,371-45,236,230 , GRCh38.p12 chr10|NW_003315935.1: 58,139-60,998 CUBNP2
    nsv4655867copy number variation1nstd186human GRCh37 chr10: 45,728,765-45,731,645 , GRCh38.p12 chr10: 45,233,317-45,236,197 , GRCh38.p12 chr10|NW_003315935.1: 58,085-60,965 CUBNP2
    nsv4644535copy number variation3nstd186human GRCh37 chr10: 45,728,770-45,731,642 , GRCh38.p12 chr10|NW_003315935.1: 58,090-60,962 , GRCh38.p12 chr10: 45,233,322-45,236,194 CUBNP2
    nsv4612930copy number variation1nstd183human GRCh37 chr10: 45,729,143-45,731,675 , GRCh38.p12 chr10|NW_003315935.1: 58,463-60,995 , GRCh38.p12 chr10: 45,233,695-45,236,227 CUBNP2
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