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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
    nsv5927577copy number variation1nstd209human GRCh38 chr18: 46,445,855-46,445,926 , GRCh37.p13 chr18: 44,025,818-44,025,889 ARK2C
    nsv5927566copy number variation1nstd209human GRCh38 chr18: 46,361,700-46,366,379 , GRCh37.p13 chr18: 43,941,663-43,946,342 ARK2C
    nsv5875760copy number variation1nstd209human GRCh38 chr18: 46,361,725-46,366,378 , GRCh37.p13 chr18: 43,941,688-43,946,341 ARK2C
    nsv5867887copy number variation1nstd209human GRCh38 chr18: 46,361,724-46,364,677 , GRCh37.p13 chr18: 43,941,687-43,944,640 ARK2C
    nsv5727047mobile element insertion1nstd211human GRCh38 chr18: 46,388,976-46,388,976 , GRCh37.p13 chr18: 43,968,939-43,968,939 ARK2C, LOC105372095
    nsv5531267copy number variation1nstd206human GRCh38 chr18: 46,397,556-46,398,952 , GRCh37.p13 chr18: 43,977,519-43,978,915 ARK2C
    nsv5522907copy number variation1nstd206human GRCh38 chr18: 46,445,855-46,445,927 , GRCh37.p13 chr18: 44,025,818-44,025,890 ARK2C
    nsv5520907copy number variation1nstd206human GRCh38 chr18: 46,361,700-46,366,380 , GRCh37.p13 chr18: 43,941,663-43,946,343 ARK2C
    nsv5514223copy number variation1nstd206human GRCh38 chr18: 46,371,684-46,374,395 , GRCh37.p13 chr18: 43,951,647-43,954,358 ARK2C
    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
    nsv5350115translocation1nstd200human GRCh38 chr18: 46,445,927-46,445,927 , GRCh38 chr18: 46,445,855-46,445,855 , GRCh37.p13 chr18: 44,025,890-44,025,890 , GRCh37.p13 chr18: 44,025,818-44,025,818 ARK2C
    nsv5350113translocation1nstd200human GRCh38 chr18: 46,397,556-46,397,556 , GRCh38 chr18: 46,398,952-46,398,952 , GRCh37.p13 chr18: 43,977,519-43,977,519 , GRCh37.p13 chr18: 43,978,915-43,978,915 ARK2C
    nsv5345345translocation1nstd200human GRCh37 chr18: 43,978,915-43,978,915 , GRCh37 chr18: 43,977,519-43,977,519 , GRCh38.p12 chr18: 46,397,556-46,397,556 , GRCh38.p12 chr18: 46,398,952-46,398,952 ARK2C
    nsv5283315copy number variation1nstd204human GRCh38.p13 chr18: 46,383,772-46,385,071 , GRCh37.p13 chr18: 43,963,735-43,965,034 ARK2C
    nsv5187377mobile element insertion1nstd203human GRCh38 chr18: 46,388,960-46,388,976 , GRCh37.p13 chr18: 43,968,923-43,968,939 ARK2C, LOC105372095
    nsv5151666mobile element insertion1nstd203human GRCh38 chr18: 46,373,421-46,373,435 , GRCh37.p13 chr18: 43,953,384-43,953,398 ARK2C
    nsv5147923mobile element insertion1nstd203human GRCh38 chr18: 46,384,436-46,384,450 , GRCh37.p13 chr18: 43,964,399-43,964,413 ARK2C
    nsv5024174copy number variation1nstd200human GRCh38 chr18: 46,383,529-46,383,867 , GRCh37.p13 chr18: 43,963,492-43,963,830 ARK2C
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