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Items: 1 to 20 of 108

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146216copy number variation1nstd232human GRCh37.p13 chr2: 90,475,722-90,475,773 , GRCh38.p12 chr2: 90,298,264-90,298,315 , GRCh38.p12 chr2|NT_187524.1: 104,208-104,259 0
    nsv7145957copy number variation1nstd232human GRCh37.p13 chr2: 90,477,443-90,477,511 , GRCh38.p12 chr2: 90,296,526-90,296,594 , GRCh38.p12 chr2|NT_187524.1: 105,929-105,997 0
    nsv5385016copy number variation1nstd186human GRCh37 chr2: 90,477,221-90,483,311 , GRCh38.p12 chr2|NT_187524.1: 105,707-111,797 , GRCh38.p12 chr2: 90,290,726-90,296,816 0
    nsv5382057copy number variation1nstd186human GRCh37 chr2: 90,478,614-90,478,868 , GRCh38.p12 chr2: 90,295,169-90,295,423 , GRCh38.p12 chr2|NT_187524.1: 107,100-107,354 0
    nsv5329882translocation1nstd200human GRCh37 chr2: 91,669,740-91,669,740 , GRCh37 chr2: 90,447,928-90,447,928 , GRCh38.p12 chr2|NT_187524.1: 76,414-76,414 , GRCh38.p12 chr2: 90,326,109-90,326,109 , GRCh38.p12 chr2|NT_187648.1: 137,735-137,735 0
    nsv4781644copy number variation1nstd200human GRCh37 chr2: 90,477,118-90,483,403 , GRCh38.p12 chr2: 90,290,623-90,296,908 , GRCh38.p12 chr2|NT_187524.1: 105,604-111,889 0
    nsv4777025copy number variation1nstd200human GRCh37 chr2: 90,478,538-90,478,975 , GRCh38.p12 chr2|NT_187524.1: 107,024-107,461 , GRCh38.p12 chr2: 90,295,093-90,295,530 0
    nsv4757280insertion1nstd199human GRCh37 chr2: 90,476,470-90,476,470 , GRCh38.p12 chr2: 90,297,567-90,297,567 , GRCh38.p12 chr2|NT_187524.1: 104,956-104,956 0
    nsv4746342copy number variation1nstd199human GRCh37 chr2: 90,475,764-90,475,820 , GRCh38.p12 chr2|NT_187524.1: 104,250-104,306 , GRCh38.p12 chr2: 90,298,217-90,298,273 0
    nsv4715613copy number variation1nstd195human GRCh37 chr2: 90,464,701-90,483,251 , GRCh38.p12 chr2: 90,290,786-90,309,336 , GRCh38.p12 chr2|NT_187524.1: 93,187-111,737 LOC101926946
    nsv4715568copy number variation2nstd195human GRCh37 chr2: 91,595,651-91,596,401 , GRCh38.p12 chr1|NT_187364.1: 6-761 , GRCh38.p12 chr2|NT_187524.1: 2,638-3,388 0
    nsv4715176copy number variation1nstd195human GRCh37 chr2: 91,605,551-91,606,101 , GRCh38.p12 chr2|NT_187524.1: 12,538-13,088 , GRCh38.p12 chr1|NT_187364.1: 9,934-10,531 0
    nsv4714848copy number variation2nstd195human GRCh37 chr2: 91,602,251-91,603,001 , GRCh38.p12 chr2|NT_187524.1: 9,238-9,988 , GRCh38.p12 chr1|NT_187364.1: 6,660-7,427 0
    nsv4711123copy number variation1nstd195human GRCh37 chr2: 91,603,951-91,604,451 , GRCh38.p12 chr2|NT_187524.1: 10,938-11,438 , GRCh38.p12 chr1|NT_187364.1: 8,358-8,844 0
    nsv4710511copy number variation1nstd195human GRCh37 chr2: 91,599,101-91,599,751 , GRCh38.p12 chr2|NT_187524.1: 6,088-6,738 , GRCh38.p12 chr1|NT_187364.1: 3,550-4,194 0
    nsv4708861copy number variation1nstd195human GRCh37 chr2: 91,613,151-91,613,851 , GRCh38.p12 chr2|NT_187524.1: 20,138-20,838 0
    nsv4707313copy number variation1nstd195human GRCh37 chr2: 91,599,001-91,599,851 , GRCh38.p12 chr2|NT_187524.1: 5,988-6,838 , GRCh38.p12 chr1|NT_187364.1: 3,450-4,300 0
    nsv4707124copy number variation1nstd195human GRCh37 chr2: 91,598,951-91,599,851 , GRCh38.p12 chr2|NT_187524.1: 5,938-6,838 , GRCh38.p12 chr1|NT_187364.1: 3,397-4,300 0
    nsv4706810copy number variation1nstd195human GRCh37 chr2: 91,603,951-91,604,601 , GRCh38.p12 chr2|NT_187524.1: 10,938-11,588 , GRCh38.p12 chr1|NT_187364.1: 8,358-8,979 0
    nsv4704499copy number variation1nstd195human GRCh37 chr2: 91,613,151-91,613,901 , GRCh38.p12 chr2|NT_187524.1: 20,138-20,888 0
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