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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137045copy number variation1nstd102humanPathogenic GRCh37 chr1: 536,777-6,012,896 , GRCh38.p12 chr1: 601,397-5,952,836 MIR200B, LOC105378608, 172 more genes
    nsv7099018copy number variation1nstd102humanPathogenic GRCh37 chr1: 1-2,580,976 , GRCh38.p12 chr1: 10,001-2,649,537 DVL1, LOC100129534, 148 more genes
    nsv7046759inversion1nstd229human GRCh38 chr1: 826,372-855,259 , GRCh37.p13 chr1: 761,752-790,639 LINC01128, LINC00115
    nsv6655851copy number variation1nstd229human GRCh38 chr1: 822,101-898,900 , GRCh37.p13 chr1: 757,481-834,280 TUBB8P11, LINC00115, 3 more genes
    nsv6655850copy number variation1nstd229human GRCh38 chr1: 822,041-898,948 , GRCh37.p13 chr1: 757,421-834,328 LINC01128, LOC107984850, 3 more genes
    nsv6655607copy number variation1nstd229human GRCh38 chr1: 818,880-922,261 , GRCh37.p13 chr1: 754,260-857,641 LOC107985728, FAM87B, 7 more genes
    nsv6655556copy number variation1nstd229human GRCh38 chr1: 805,291-861,419 , GRCh37.p13 chr1: 740,671-796,799 LINC01128, LOC107984850, 3 more genes
    nsv6655450copy number variation1nstd229human GRCh38 chr1: 793,983-893,058 , GRCh37.p13 chr1: 729,363-828,438 LOC107984850, LINC00115, 5 more genes
    nsv6655245copy number variation1nstd229human GRCh38 chr1: 786,558-837,631 , GRCh37.p13 chr1: 721,938-773,011 LINC01128, FAM87B, 2 more genes
    nsv6655224copy number variation1nstd229human GRCh38 chr1: 779,836-875,281 , GRCh37.p13 chr1: 715,216-810,661 LINC01128, TUBB8P11, 5 more genes
    nsv6655165copy number variation1nstd229human GRCh38 chr1: 785,101-906,500 , GRCh37.p13 chr1: 720,481-841,880 LINC01409, TUBB8P11, 6 more genes
    nsv6655052copy number variation1nstd229human GRCh38 chr1: 818,999-1,165,510 , GRCh37.p13 chr1: 754,379-1,100,890 HES4, LOC105378948, 22 more genes
    nsv6626515copy number variation8nstd224human GRCh37 chr1: 759,036-846,808 , GRCh38.p12 chr1: 823,656-911,428 LINC00115, FAM41C, 4 more genes
    nsv6626514copy number variation1nstd224human GRCh37 chr1: 752,566-909,917 , GRCh38.p12 chr1: 817,186-974,537 LINC00115, LINC02593, 12 more genes
    nsv6626470copy number variation13nstd224human GRCh37 chr1: 752,566-838,555 , GRCh38.p12 chr1: 817,186-903,175 LINC00115, FAM41C, 5 more genes
    nsv6626467copy number variation5nstd224human GRCh37 chr1: 727,841-851,390 , GRCh38.p12 chr1: 792,461-916,010 LINC00115, FAM41C, 7 more genes
    nsv6626466copy number variation12nstd224human GRCh37 chr1: 727,841-846,808 , GRCh38.p12 chr1: 792,461-911,428 LINC00115, FAM41C, 6 more genes
    nsv6626396copy number variation40nstd224human GRCh37 chr1: 752,721-846,808 , GRCh38.p12 chr1: 817,341-911,428 LINC00115, FAM41C, 5 more genes
    nsv6626395copy number variation1nstd224human GRCh37 chr1: 752,566-866,438 , GRCh38.p12 chr1: 817,186-931,058 LINC00115, FAM41C, 8 more genes
    nsv6626388copy number variation2nstd224human GRCh37 chr1: 727,841-840,753 , GRCh38.p12 chr1: 792,461-905,373 LINC00115, FAM41C, 6 more genes
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