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Items: 1 to 20 of 871

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077560inversion1nstd229human GRCh38 chr11: 28,134,625-28,187,449 , GRCh37.p13 chr11: 28,156,172-28,208,996 METTL15, ATP5MGP8
    nsv7075847inversion1nstd229human GRCh38 chr11: 28,157,226-28,247,093 , GRCh37.p13 chr11: 28,178,773-28,268,640 METTL15
    nsv7074285inversion1nstd229human GRCh38 chr11: 25,121,393-29,376,238 , GRCh37.p13 chr11: 25,142,939-29,397,785 RPL37AP7, LOC107984367, 40 more genes
    nsv7074064inversion1nstd229human GRCh38 chr11: 27,951,557-29,398,351 , GRCh37.p13 chr11: 27,973,104-29,419,898 LOC105376604, KIF18A, 12 more genes
    nsv7070055inversion1nstd229human GRCh38 chr11: 28,296,603-28,297,072 , GRCh37.p13 chr11: 28,318,150-28,318,619 METTL15
    nsv7067720inversion1nstd229human GRCh38 chr11: 28,504,719-28,509,719 , GRCh37.p13 chr11: 28,526,266-28,531,266 METTL15
    nsv7066299inversion1nstd229human GRCh38 chr11: 28,323,029-28,323,114 , GRCh37.p13 chr11: 28,344,576-28,344,661 METTL15
    nsv7063041inversion1nstd229human GRCh38 chr11: 28,163,150-28,172,181 , GRCh37.p13 chr11: 28,184,697-28,193,728 METTL15
    nsv7059862inversion1nstd229human GRCh38 chr11: 28,121,695-28,121,771 , GRCh37.p13 chr11: 28,143,242-28,143,318 METTL15
    nsv7059233inversion1nstd229human GRCh38 chr11: 28,513,981-28,650,254 , GRCh37.p13 chr11: 28,535,528-28,671,801 LINC02758, METTL15
    nsv6918048copy number variation1nstd229human GRCh38 chr11: 28,462,758-28,470,735 , GRCh37.p13 chr11: 28,484,305-28,492,282 METTL15
    nsv6917919copy number variation1nstd229human GRCh38 chr11: 28,126,345-28,130,287 , GRCh37.p13 chr11: 28,147,892-28,151,834 METTL15
    nsv6917496copy number variation1nstd229human GRCh38 chr11: 28,197,561-28,292,444 , GRCh37.p13 chr11: 28,219,108-28,313,991 RN7SKP158, RPS15AP31, 1 more genes
    nsv6916941copy number variation1nstd229human GRCh38 chr11: 28,010,901-28,223,000 , GRCh37.p13 chr11: 28,032,448-28,244,547 ATP5MGP8, METTL15, 2 more genes
    nsv6916658copy number variation1nstd229human GRCh38 chr11: 28,443,075-28,448,127 , GRCh37.p13 chr11: 28,464,622-28,469,674 METTL15
    nsv6916004copy number variation1nstd229human GRCh38 chr11: 28,147,636-28,297,641 , GRCh37.p13 chr11: 28,169,183-28,319,188 RN7SKP158, METTL15, 1 more genes
    nsv6915988copy number variation1nstd229human GRCh38 chr11: 28,152,545-28,312,554 , GRCh37.p13 chr11: 28,174,092-28,334,101 RPS15AP31, RN7SKP158, 1 more genes
    nsv6915965copy number variation1nstd229human GRCh38 chr11: 28,202,387-28,256,924 , GRCh37.p13 chr11: 28,223,934-28,278,471 METTL15
    nsv6915963copy number variation1nstd229human GRCh38 chr11: 28,262,801-28,286,600 , GRCh37.p13 chr11: 28,284,348-28,308,147 METTL15, RPS15AP31
    nsv6914609copy number variation1nstd229human GRCh38 chr11: 28,126,301-28,130,300 , GRCh37.p13 chr11: 28,147,848-28,151,847 METTL15
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