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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7062606inversion1nstd229human GRCh38 chr19: 10,024,335-10,946,724 , GRCh37.p13 chr19: 10,135,011-11,057,400 FDX2, ICAM4, 48 more genes
    nsv7061047inversion1nstd229human GRCh38 chr19: 10,123,796-11,885,300 , GRCh37.p13 chr19: 10,234,472-11,996,115 QTRT1, ZNF653, 82 more genes
    nsv6998259copy number variation1nstd229human GRCh38 chr19: 10,046,601-11,033,768 , GRCh37.p13 chr19: 10,157,277-11,144,444 MRPL4, QTRT1, 49 more genes
    nsv6534802copy number variation1nstd223human GRCh38 chr19: 10,218,261-10,219,513 , GRCh37.p13 chr19: 10,328,937-10,330,189 S1PR2
    nsv6528634copy number variation1nstd223human GRCh38 chr19: 10,222,001-10,223,200 , GRCh37.p13 chr19: 10,332,677-10,333,876 S1PR2
    nsv6523625copy number variation1nstd223human GRCh38 chr19: 10,219,168-10,220,322 , GRCh37.p13 chr19: 10,329,844-10,330,998 S1PR2
    nsv6515612copy number variation1nstd223human GRCh38 chr19: 10,228,937-10,229,626 , GRCh37.p13 chr19: 10,339,613-10,340,302 MIR4322, S1PR2
    nsv6291543copy number variation1nstd102humanUncertain significance GRCh37 chr19: 9,941,033-11,739,567 , GRCh38.p12 chr19: 9,830,357-11,628,752 KRI1, SHFL, 88 more genes
    nsv6133698copy number variation1nstd213human GRCh37 chr19: 2,900,000-11,490,001 , GRCh38.p12 chr19: 2,900,002-11,379,325 , TLE5, 341 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv5945670copy number variation1nstd209human GRCh38 chr19: 10,230,560-10,230,613 , GRCh37.p13 chr19: 10,341,236-10,341,289 MIR4322, S1PR2
    nsv5942141copy number variation1nstd209human GRCh38 chr19: 10,230,091-10,230,202 , GRCh37.p13 chr19: 10,340,767-10,340,878 MIR4322, S1PR2
    nsv5529106copy number variation1nstd206human GRCh38 chr19: 10,230,414-10,230,486 , GRCh37.p13 chr19: 10,341,090-10,341,162 S1PR2, MIR4322
    nsv5527259copy number variation1nstd206human GRCh38 chr19: 10,230,835-10,231,249 , GRCh37.p13 chr19: 10,341,511-10,341,925 S1PR2, MIR4322
    nsv5523944copy number variation1nstd206human GRCh38 chr19: 10,230,425-10,230,517 , GRCh37.p13 chr19: 10,341,101-10,341,193 S1PR2, MIR4322
    nsv5288069copy number variation1nstd204human GRCh38.p13 chr19: 10,216,408-10,327,822 , GRCh37.p13 chr19: 10,327,084-10,438,498 FDX2, MRPL4, 9 more genes
    nsv5284255copy number variation1nstd204human GRCh38.p13 chr19: 10,061,101-10,331,300 , GRCh37.p13 chr19: 10,171,777-10,441,976 ICAM1, ICAM4, 19 more genes
    nsv5011594copy number variation1nstd200human GRCh38 chr19: 10,218,231-10,219,527 , GRCh37.p13 chr19: 10,328,907-10,330,203 S1PR2
    nsv4624262copy number variation1nstd183human GRCh37 chr19: 10,218,959-10,370,939 , GRCh38.p12 chr19: 10,108,283-10,260,263 EIF3G, MIR4322, 9 more genes
    nsv4269657copy number variation1nstd166human GRCh37.p13 chr19: 10,328,938-10,330,191 , GRCh38.p12 chr19: 10,218,262-10,219,515 S1PR2
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