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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7016006copy number variation1nstd229human GRCh38 chr18: 36,125,901-36,161,600 , GRCh37.p13 chr18: 33,705,864-33,741,563 SLC39A6, ELP2
    nsv7009293copy number variation1nstd229human GRCh38 chr18: 34,453,177-37,158,337 , GRCh37.p13 chr18: 32,033,141-34,738,300 LOC105372061, RNU4-3P, 31 more genes
    nsv7004976copy number variation1nstd229human GRCh38 chr18: 36,115,556-36,124,946 , GRCh37.p13 chr18: 33,695,519-33,704,909 SLC39A6
    nsv7000746copy number variation1nstd229human GRCh38 chr18: 36,115,910-36,119,811 , GRCh37.p13 chr18: 33,695,873-33,699,774 SLC39A6
    nsv6579756inversion1nstd223human GRCh38 chr18: 36,127,385-36,127,790 , GRCh37.p13 chr18: 33,707,348-33,707,753 SLC39A6
    nsv6529054copy number variation1nstd223human GRCh38 chr18: 36,115,909-36,119,810 , GRCh37.p13 chr18: 33,695,872-33,699,773 SLC39A6
    nsv6517543copy number variation1nstd223human GRCh38 chr18: 36,115,554-36,124,943 , GRCh37.p13 chr18: 33,695,517-33,704,906 SLC39A6
    nsv6315530copy number variation1nstd102humanPathogenic GRCh37 chr18: 1-78,077,248 , GRCh38.p12 chr18: 10,001-80,259,271 LOC105372145, LOC105372016, 947 more genes
    nsv6314722copy number variation1nstd102humanPathogenic GRCh37 chr18: 1,262,334-53,254,751 , GRCh38.p12 chr18: 1,262,333-55,587,520 LOC107985176, ZNF521, 632 more genes
    nsv6291602copy number variation1nstd102humanUncertain significance GRCh37 chr18: 33,571,456-34,552,945 , GRCh38.p12 chr18: 35,991,493-36,972,982 ELP2, COSMOC, 10 more genes
    nsv6133439copy number variation1nstd213human GRCh37 chr18: 28,680,000-49,600,001 , GRCh38.p12 chr18: 31,100,037-52,073,631 ATP5F1A, DSC1, 240 more genes
    nsv6133334copy number variation1nstd213human GRCh37 chr18: 32,810,000-34,010,001 , GRCh38.p12 chr18: 35,230,036-36,430,038 GALNT1, ZNF24, 23 more genes
    nsv6133333copy number variation1nstd213human GRCh37 chr18: 27,400,000-52,060,001 , GRCh38.p12 chr18: 29,820,035-54,532,766 ATP5F1A, DCC, 259 more genes
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv6110538insertion1nstd212human GRCh38 chr18: 36,108,478-36,108,478 , GRCh37.p13 chr18: 33,688,441-33,688,441 SLC39A6
    nsv6107779inversion1nstd212human GRCh38 chr18: 34,743,532-36,146,243 , GRCh37.p13 chr18: 32,323,496-33,726,206 , DTNA, 22 more genes
    nsv5704279mobile element insertion2nstd211human GRCh38 chr18: 36,119,603-36,119,603 , GRCh37.p13 chr18: 33,699,566-33,699,566 SLC39A6
    nsv5655809insertion1nstd207human GRCh38 chr18: 36,119,591-36,119,591 , GRCh37.p13 chr18: 33,699,554-33,699,554 SLC39A6
    nsv5421764mobile element insertion1nstd206human GRCh38 chr18: 36,119,603-36,119,654 , GRCh37.p13 chr18: 33,699,566-33,699,617 SLC39A6
    nsv5298773copy number variation1nstd204human GRCh38.p13 chr18: 36,084,713-36,115,674 , GRCh37.p13 chr18: 33,664,676-33,695,637 SLC39A6
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