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Items: 1 to 20 of 227

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076106inversion1nstd229human GRCh38 chr14: 44,990,653-45,275,284 , GRCh37.p13 chr14: 45,459,856-45,744,487 TOGARAM1, FANCM, 7 more genes
    nsv7063014inversion1nstd229human GRCh38 chr14: 40,555,754-49,209,932 , GRCh37.p13 chr14: 41,024,959-49,676,650 LRFN5, LRFN5-DT, 62 more genes
    nsv7060156inversion1nstd229human GRCh38 chr14: 44,666,466-45,365,086 , GRCh37.p13 chr14: 45,135,669-45,834,289 FKBP3, KLHL28, 15 more genes
    nsv6957952copy number variation1nstd229human GRCh38 chr14: 45,152,080-45,286,979 , GRCh37.p13 chr14: 45,621,283-45,756,182 FANCM, LOC107984674, 2 more genes
    nsv6957426copy number variation1nstd229human GRCh38 chr14: 45,237,566-45,965,336 , GRCh37.p13 chr14: 45,706,769-46,434,539 DNAJC19P9, LOC105378177, 8 more genes
    nsv6955670copy number variation1nstd229human GRCh38 chr14: 45,218,856-45,218,923 , GRCh37.p13 chr14: 45,688,059-45,688,126 MIS18BP1
    nsv6953305copy number variation1nstd229human GRCh38 chr14: 44,520,856-45,505,567 , GRCh37.p13 chr14: 44,990,059-45,974,770 DOCK11P1, LOC101927418, 19 more genes
    nsv6952502copy number variation1nstd229human GRCh38 chr14: 45,116,128-45,756,370 , GRCh37.p13 chr14: 45,585,331-46,225,573 LOC105370475, LOC107984644, 10 more genes
    nsv6947464copy number variation1nstd229human GRCh38 chr14: 45,181,686-45,233,723 , GRCh37.p13 chr14: 45,650,889-45,702,926 MIS18BP1, FANCM
    nsv6945049copy number variation1nstd229human GRCh38 chr14: 45,245,573-45,248,946 , GRCh37.p13 chr14: 45,714,776-45,718,149 MIS18BP1
    nsv6944990copy number variation1nstd229human GRCh38 chr14: 44,969,026-45,213,202 , GRCh37.p13 chr14: 45,438,229-45,682,405 SNORD127, FKBP3, 5 more genes
    nsv6943362copy number variation1nstd229human GRCh38 chr14: 45,088,701-45,374,100 , GRCh37.p13 chr14: 45,557,904-45,843,303 SNORD127, LOC105370475, 7 more genes
    nsv6942551copy number variation1nstd229human GRCh38 chr14: 45,212,914-45,216,105 , GRCh37.p13 chr14: 45,682,117-45,685,308 MIS18BP1
    nsv6938445copy number variation1nstd229human GRCh38 chr14: 45,234,287-45,246,708 , GRCh37.p13 chr14: 45,703,490-45,715,911 MIS18BP1
    nsv6622732copy number variation1nstd224human GRCh37 chr14: 45,693,239-45,713,358 , GRCh38.p12 chr14: 45,224,036-45,244,155 MIS18BP1
    nsv6622730copy number variation1nstd224human GRCh37 chr14: 45,620,721-45,753,772 , GRCh38.p12 chr14: 45,151,518-45,284,569 FANCM, MIS18BP1, 2 more genes
    nsv6622661copy number variation1nstd224human GRCh37 chr14: 45,702,167-45,801,798 , GRCh38.p12 chr14: 45,232,964-45,332,595 RNU6-552P, LOC107984674, 2 more genes
    nsv6622313copy number variation1nstd224human GRCh37 chr14: 45,654,467-45,691,116 , GRCh38.p12 chr14: 45,185,264-45,221,913 FANCM, MIS18BP1
    nsv6590271inversion1nstd223human GRCh38 chr14: 45,240,185-45,240,556 , GRCh37.p13 chr14: 45,709,388-45,709,759 MIS18BP1
    nsv6576170inversion1nstd223human GRCh38 chr14: 45,249,273-45,249,600 , GRCh37.p13 chr14: 45,718,476-45,718,803 MIS18BP1
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