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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5970228inversion1nstd209human GRCh38 chr18: 42,666,448-47,133,105 , GRCh37.p13 chr18: 40,246,413-44,659,476 , ATP5F1A, 50 more genes
    nsv5928309copy number variation1nstd209human GRCh38 chr18: 45,461,084-45,461,990 , GRCh37.p13 chr18: 43,041,049-43,041,955 SLC14A2-AS1, SLC14A2
    nsv5526589copy number variation1nstd206human GRCh38 chr18: 45,500,922-45,504,896 , GRCh37.p13 chr18: 43,080,887-43,084,861 SLC14A2-AS1, SLC14A2
    nsv5515896copy number variation1nstd206human GRCh38 chr18: 45,506,340-45,506,470 , GRCh37.p13 chr18: 43,086,305-43,086,435 SLC14A2, SLC14A2-AS1
    nsv5381046copy number variation2nstd102humanUncertain significance GRCh37 chr18: 42,281,312-45,423,127 , GRCh38.p12 chr18: 44,701,347-47,896,756 HDHD2, RNU6-1131P, 45 more genes
    nsv5150361mobile element insertion1nstd203human GRCh38 chr18: 45,468,440-45,468,454 , GRCh37.p13 chr18: 43,048,405-43,048,419 SLC14A2-AS1, SLC14A2
    nsv5143468mobile element insertion1nstd203human GRCh38 chr18: 45,434,751-45,434,763 , GRCh37.p13 chr18: 43,014,716-43,014,728 SLC14A2-AS1, SLC14A2
    nsv5017886copy number variation1nstd200human GRCh38 chr18: 45,466,111-45,466,938 , GRCh37.p13 chr18: 43,046,076-43,046,903 SLC14A2, SLC14A2-AS1
    nsv4676219copy number variation1nstd102humanPathogenic GRCh37 chr18: 41,630,585-45,107,905 , GRCh38.p12 chr18: 44,050,620-47,581,534 HAUS1, KATNAL2, 48 more genes
    nsv4676156copy number variation1nstd102humanPathogenic GRCh37 chr18: 39,800,804-44,365,152 , GRCh38.p12 chr18: 42,220,839-46,785,189 LOC105372089, RPS21P6, 40 more genes
    nsv4676155copy number variation1nstd102humanPathogenic GRCh37 chr18: 20,689,919-49,455,212 , GRCh38.p12 chr18: 23,109,955-51,928,842 KLHL14, RPL23AP77, 318 more genes
    nsv4628009copy number variation1nstd183human GRCh37 chr18: 43,013,428-43,014,194 , GRCh38.p12 chr18: 45,433,463-45,434,229 , GRCh38.p12 chr18|NW_019805502.1: 53,578-54,344 SLC14A2-AS1, SLC14A2
    nsv4565923mobile element insertion1nstd166human GRCh37.p13 chr18: 43,018,757-43,018,757 , GRCh38.p12 chr18|NW_019805502.1: 58,907-58,907 , GRCh38.p12 chr18: 45,438,792-45,438,792 SLC14A2-AS1, SLC14A2
    nsv4457501copy number variation1nstd102humanUncertain significance GRCh37 chr18: 42,077,361-43,132,127 , GRCh38.p12 chr18: 44,497,396-45,552,162 LINC01478, MIR4319, 9 more genes
    nsv4336672sequence alteration1nstd166human GRCh37.p13 chr18: 21,176,191-70,772,863 , GRCh38.p12 chr18: 23,596,227-73,105,628 , CDH2, 557 more genes
    nsv4266639copy number variation1nstd166human GRCh37.p13 chr18: 43,087,220-43,096,828 , GRCh38.p12 chr18|NW_019805502.1: 127,388-136,997 , GRCh38.p12 chr18: 45,507,255-45,516,863 SLC14A2-AS1, LOC112268408, 1 more genes
    nsv4261747copy number variation1nstd166human GRCh37.p13 chr18: 43,074,254-43,075,179 , GRCh38.p12 chr18: 45,494,289-45,495,214 , GRCh38.p12 chr18|NW_019805502.1: 114,404-115,329 SLC14A2, SLC14A2-AS1, 1 more genes
    nsv4258879copy number variation1nstd166human GRCh37.p13 chr18: 43,014,591-43,014,647 , GRCh38.p12 chr18: 45,434,626-45,434,682 , GRCh38.p12 chr18|NW_019805502.1: 54,741-54,797 SLC14A2, SLC14A2-AS1
    nsv3963706insertion1nstd168human GRCh38 chr18: 45,436,408-45,437,039 , GRCh37.p13 chr18: 43,016,373-43,017,004 SLC14A2, SLC14A2-AS1
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