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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074285inversion1nstd229human GRCh38 chr11: 25,121,393-29,376,238 , GRCh37.p13 chr11: 25,142,939-29,397,785 RPL37AP7, LOC107984367, 40 more genes
    nsv7070460inversion1nstd229human GRCh38 chr11: 21,520,035-27,618,155 , GRCh37.p13 chr11: 21,541,581-27,639,702 RPS25P1, LOC105376598, 48 more genes
    nsv6914983copy number variation1nstd229human GRCh38 chr11: 25,587,958-25,588,256 , GRCh37.p13 chr11: 25,609,504-25,609,802 RPL36AP40
    nsv6914133copy number variation1nstd229human GRCh38 chr11: 25,563,474-25,910,598 , GRCh37.p13 chr11: 25,585,020-25,932,145 LOC107984367, LINC02699, 1 more genes
    nsv6914055copy number variation1nstd229human GRCh38 chr11: 25,585,001-25,608,100 , GRCh37.p13 chr11: 25,606,547-25,629,646 RPL36AP40
    nsv6913754copy number variation1nstd229human GRCh38 chr11: 25,547,901-25,597,100 , GRCh37.p13 chr11: 25,569,447-25,618,646 RPL36AP40
    nsv6912421copy number variation1nstd229human GRCh38 chr11: 25,372,733-25,610,671 , GRCh37.p13 chr11: 25,394,279-25,632,217 RPL36AP40
    nsv6911407copy number variation1nstd229human GRCh38 chr11: 25,549,078-25,606,165 , GRCh37.p13 chr11: 25,570,624-25,627,711 RPL36AP40
    nsv6909829copy number variation1nstd229human GRCh38 chr11: 25,575,759-25,620,547 , GRCh37.p13 chr11: 25,597,305-25,642,093 RPL36AP40
    nsv6909270copy number variation1nstd229human GRCh38 chr11: 25,579,901-25,609,500 , GRCh37.p13 chr11: 25,601,447-25,631,046 RPL36AP40
    nsv6908351copy number variation1nstd229human GRCh38 chr11: 25,561,956-25,730,210 , GRCh37.p13 chr11: 25,583,502-25,751,757 LOC107984367, RPL36AP40
    nsv6907687copy number variation1nstd229human GRCh38 chr11: 25,546,901-25,596,700 , GRCh37.p13 chr11: 25,568,447-25,618,246 RPL36AP40
    nsv6907264copy number variation1nstd229human GRCh38 chr11: 25,583,701-25,609,300 , GRCh37.p13 chr11: 25,605,247-25,630,846 RPL36AP40
    nsv6907034copy number variation1nstd229human GRCh38 chr11: 25,571,351-25,814,472 , GRCh37.p13 chr11: 25,592,897-25,836,019 RPL36AP40, LINC02699, 1 more genes
    nsv6906158copy number variation1nstd229human GRCh38 chr11: 18,831,701-26,837,040 , GRCh37.p13 chr11: 18,853,248-26,858,587 HTATIP2, LINC02686, 68 more genes
    nsv6905709copy number variation1nstd229human GRCh38 chr11: 25,585,401-25,607,800 , GRCh37.p13 chr11: 25,606,947-25,629,346 RPL36AP40
    nsv6904608copy number variation1nstd229human GRCh38 chr11: 25,562,421-25,588,435 , GRCh37.p13 chr11: 25,583,967-25,609,981 RPL36AP40
    nsv6903444copy number variation1nstd229human GRCh38 chr11: 24,768,508-26,268,124 , GRCh37.p13 chr11: 24,790,054-26,289,671 ANO3, LOC100533706, 5 more genes
    nsv6903355copy number variation1nstd229human GRCh38 chr11: 25,530,877-26,656,773 , GRCh37.p13 chr11: 25,552,423-26,678,320 LOC105376598, LOC107987160, 7 more genes
    nsv6901880copy number variation1nstd229human GRCh38 chr11: 25,547,401-25,598,900 , GRCh37.p13 chr11: 25,568,947-25,620,446 RPL36AP40
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