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Items: 1 to 20 of 947

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056028inversion1nstd229human GRCh38 chr2: 99,846,331-99,860,160 , GRCh37.p13 chr2: 100,462,793-100,476,622 AFF3
    nsv7051246inversion1nstd229human GRCh38 chr2: 99,001,430-99,852,801 , GRCh37.p13 chr2: 99,617,893-100,469,263 EIF5B, MITD1, 12 more genes
    nsv7048927inversion1nstd229human GRCh38 chr2: 99,846,400-99,860,165 , GRCh37.p13 chr2: 100,462,862-100,476,627 AFF3
    nsv7048876inversion1nstd229human GRCh38 chr2: 99,916,080-99,916,092 , GRCh37.p13 chr2: 100,532,542-100,532,554 AFF3
    nsv7047423inversion1nstd229human GRCh38 chr2: 100,064,365-100,070,221 , GRCh37.p13 chr2: 100,680,827-100,686,683 AFF3
    nsv7043267inversion1nstd229human GRCh38 chr2: 99,941,940-99,942,002 , GRCh37.p13 chr2: 100,558,402-100,558,464 AFF3
    nsv6697981copy number variation1nstd229human GRCh38 chr2: 99,792,694-99,815,959 , GRCh37.p13 chr2: 100,409,156-100,432,421 AFF3
    nsv6697882copy number variation1nstd229human GRCh38 chr2: 100,130,671-100,137,393 , GRCh37.p13 chr2: 100,747,133-100,753,855 AFF3
    nsv6697610copy number variation1nstd229human GRCh38 chr2: 99,418,732-99,583,219 , GRCh37.p13 chr2: 100,035,194-100,199,681 REV1, AFF3
    nsv6696821copy number variation1nstd229human GRCh38 chr2: 100,106,299-100,276,473 , GRCh37.p13 chr2: 100,722,761-100,892,935 AFF3, LONRF2, 1 more genes
    nsv6696565copy number variation1nstd229human GRCh38 chr2: 99,608,885-99,609,081 , GRCh37.p13 chr2: 100,225,347-100,225,543 AFF3
    nsv6696402copy number variation1nstd229human GRCh38 chr2: 99,984,222-99,984,337 , GRCh37.p13 chr2: 100,600,684-100,600,799 AFF3
    nsv6695887copy number variation1nstd229human GRCh38 chr2: 99,662,903-100,342,170 , GRCh37.p13 chr2: 100,279,365-100,958,632 LOC105373504, LINC01104, 2 more genes
    nsv6695760copy number variation1nstd229human GRCh38 chr2: 99,941,073-99,959,633 , GRCh37.p13 chr2: 100,557,535-100,576,095 AFF3
    nsv6695675copy number variation1nstd229human GRCh38 chr2: 100,051,717-100,055,959 , GRCh37.p13 chr2: 100,668,179-100,672,421 AFF3
    nsv6695651copy number variation1nstd229human GRCh38 chr2: 99,650,301-99,651,800 , GRCh37.p13 chr2: 100,266,763-100,268,262 AFF3
    nsv6695332copy number variation1nstd229human GRCh38 chr2: 99,951,796-99,956,573 , GRCh37.p13 chr2: 100,568,258-100,573,035 AFF3
    nsv6695197copy number variation1nstd229human GRCh38 chr2: 99,718,601-99,726,000 , GRCh37.p13 chr2: 100,335,063-100,342,462 AFF3
    nsv6695097copy number variation1nstd229human GRCh38 chr2: 99,828,391-99,832,036 , GRCh37.p13 chr2: 100,444,853-100,448,498 AFF3
    nsv6694867copy number variation1nstd229human GRCh38 chr2: 99,755,709-99,767,081 , GRCh37.p13 chr2: 100,372,171-100,383,543 AFF3
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