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Items: 1 to 20 of 249

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137096copy number variation1nstd102humanLikely benign GRCh37 chr11: 5,094,756-5,785,959 , GRCh38.p12 chr11: 5,073,526-5,764,729 OR51J1, OLFM5P, 52 more genes
    nsv6917937copy number variation1nstd229human GRCh38 chr11: 5,738,698-5,753,526 , GRCh37.p13 chr11: 5,759,928-5,774,756 OR52N4, OR56B1
    nsv6917862copy number variation1nstd229human GRCh38 chr11: 5,738,858-5,741,136 , GRCh37.p13 chr11: 5,760,088-5,762,366 OR56B1, OR52N4
    nsv6917470copy number variation1nstd229human GRCh38 chr11: 5,738,901-5,741,100 , GRCh37.p13 chr11: 5,760,131-5,762,330 OR56B1, OR52N4
    nsv6917011copy number variation1nstd229human GRCh38 chr11: 2,693,282-9,207,515 , GRCh37.p13 chr11: 2,714,512-9,229,062 LOC105376526, OR51E2, 279 more genes
    nsv6910339copy number variation1nstd229human GRCh38 chr11: 5,737,301-5,750,900 , GRCh37.p13 chr11: 5,758,531-5,772,130 OR56B1, OR52N4
    nsv6902633copy number variation1nstd229human GRCh38 chr11: 5,538,086-5,938,396 , GRCh37.p13 chr11: 5,559,316-5,959,626 OR52N1, OR52N4, 26 more genes
    nsv6637864copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,616-8,250,724 , GRCh38.p12 chr11: 230,616-8,229,177 PNPLA2, OR52H1, 372 more genes
    nsv6621251copy number variation1nstd224human GRCh37 chr11: 5,727,822-5,995,159 , GRCh38.p12 chr11: 5,706,592-5,973,929 TRIM22, OR52N1, 17 more genes
    nsv6453437copy number variation1nstd223human GRCh38 chr11: 5,738,857-5,741,135 , GRCh37.p13 chr11: 5,760,087-5,762,365 OR56B1, OR52N4
    nsv6441849copy number variation1nstd223human GRCh38 chr11: 5,588,812-6,011,442 , GRCh37.p13 chr11: 5,610,042-6,032,672 OR52N5, OR52N4, 26 more genes
    nsv6437487copy number variation1nstd223human GRCh38 chr11: 5,568,264-6,075,481 , GRCh37.p13 chr11: 5,589,494-6,096,711 TRIM34, OR52E6, 33 more genes
    nsv6436757copy number variation1nstd223human GRCh38 chr11: 5,618,722-5,835,186 , GRCh37.p13 chr11: 5,639,952-5,856,416 OR56B2P, OR52P1, 12 more genes
    nsv6315535copy number variation1nstd102humanPathogenic GRCh37 chr11: 230,615-26,881,146 , GRCh38.p12 chr11: 230,615-26,859,599 OR52Q1P, RNU6-593P, 630 more genes
    nsv6021855copy number variation1nstd212human GRCh38 chr11: 5,738,857-5,741,134 , GRCh37.p13 chr11: 5,760,087-5,762,364 OR52N4, OR56B1
    nsv5908934copy number variation1nstd209human GRCh38 chr11: 5,738,857-5,741,134 , GRCh37.p13 chr11: 5,760,087-5,762,364 OR56B1, OR52N4
    nsv5867041copy number variation1nstd209human GRCh38 chr11: 5,738,918-5,741,167 , GRCh37.p13 chr11: 5,760,148-5,762,397 OR52N4, OR56B1
    nsv5713971mobile element insertion2nstd211human GRCh38 chr11: 5,738,490-5,738,490 , GRCh37.p13 chr11: 5,759,720-5,759,720 OR52N4, OR56B1
    nsv5599028copy number variation1nstd207human GRCh38 chr11: 5,738,857-5,741,133 , GRCh37.p13 chr11: 5,760,087-5,762,363 OR56B1, OR52N4
    nsv5508311copy number variation1nstd206human GRCh38 chr11: 5,738,857-5,741,135 , GRCh37.p13 chr11: 5,760,087-5,762,365 OR52N4, OR56B1
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