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Items: 1 to 20 of 407

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077729inversion1nstd229human GRCh38 chr9: 94,417,509-96,970,614 , GRCh37.p13 chr9: 97,179,791-99,732,896 HSD17B3-AS1, ERCC6L2, 60 more genes
    nsv7075365inversion1nstd229human GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272 PCAT7, ANKS6, 128 more genes
    nsv7061823inversion1nstd229human GRCh38 chr9: 94,710,575-96,645,135 , GRCh37.p13 chr9: 97,472,857-99,407,417 LOC105376163, LINC00092, 42 more genes
    nsv6877603copy number variation1nstd229human GRCh38 chr9: 96,535,710-96,535,795 , GRCh37.p13 chr9: 99,297,992-99,298,077 CDC14B
    nsv6875294copy number variation1nstd229human GRCh38 chr9: 96,567,487-96,645,140 , GRCh37.p13 chr9: 99,329,769-99,407,422 PRXL2C, CDC14B, 1 more genes
    nsv6873778copy number variation1nstd229human GRCh38 chr9: 96,531,609-96,531,654 , GRCh37.p13 chr9: 99,293,891-99,293,936 CDC14B
    nsv6872880copy number variation1nstd229human GRCh38 chr9: 96,529,508-96,530,178 , GRCh37.p13 chr9: 99,291,790-99,292,460 CDC14B
    nsv6871412copy number variation1nstd229human GRCh38 chr9: 96,507,001-96,508,300 , GRCh37.p13 chr9: 99,269,283-99,270,582 CDC14B
    nsv6870291copy number variation1nstd229human GRCh38 chr9: 96,566,201-96,753,000 , GRCh37.p13 chr9: 99,328,483-99,515,282 LOC105376163, PRXL2C, 3 more genes
    nsv6868486copy number variation1nstd229human GRCh38 chr9: 96,581,470-96,581,522 , GRCh37.p13 chr9: 99,343,752-99,343,804 CDC14B
    nsv6867833copy number variation1nstd229human GRCh38 chr9: 96,332,401-96,753,000 , GRCh37.p13 chr9: 99,094,683-99,515,282 SLC35D2, LOC105376163, 7 more genes
    nsv6866127copy number variation1nstd229human GRCh38 chr9: 96,496,857-96,499,497 , GRCh37.p13 chr9: 99,259,139-99,261,779 CDC14B
    nsv6862475copy number variation1nstd229human GRCh38 chr9: 96,619,301-96,736,300 , GRCh37.p13 chr9: 99,381,583-99,498,582 PRXL2C, CDC14B, 1 more genes
    nsv6862327copy number variation1nstd229human GRCh38 chr9: 96,531,405-96,531,479 , GRCh37.p13 chr9: 99,293,687-99,293,761 CDC14B
    nsv6861697copy number variation1nstd229human GRCh38 chr9: 96,542,221-96,542,264 , GRCh37.p13 chr9: 99,304,503-99,304,546 CDC14B
    nsv6861314copy number variation1nstd229human GRCh38 chr9: 96,605,068-96,738,478 , GRCh37.p13 chr9: 99,367,350-99,500,760 LOC105376163, PRXL2C, 2 more genes
    nsv6860630copy number variation1nstd229human GRCh38 chr9: 96,494,075-96,531,432 , GRCh37.p13 chr9: 99,256,357-99,293,714 CDC14B
    nsv6859598copy number variation1nstd229human GRCh38 chr9: 96,518,400-96,521,327 , GRCh37.p13 chr9: 99,280,682-99,283,609 CDC14B
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6633558copy number variation1nstd224human GRCh37 chr9: 99,262,296-99,606,529 , GRCh38.p12 chr9: 96,500,014-96,844,247 CDC14B, ZNF510, 4 more genes
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