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Items: 1 to 20 of 296

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076635inversion1nstd229human GRCh38 chr12: 100,477,855-100,483,839 , GRCh37.p13 chr12: 100,871,633-100,877,617 NR1H4
    nsv7076221inversion1nstd229human GRCh38 chr12: 100,472,775-100,484,071 , GRCh37.p13 chr12: 100,866,553-100,877,849 NR1H4
    nsv7074674inversion1nstd229human GRCh38 chr12: 100,072,817-104,989,567 , GRCh37.p13 chr12: 100,466,595-105,383,345 SYCP3, GOLGA2P5, 84 more genes
    nsv7072556inversion1nstd229human GRCh38 chr12: 100,468,751-100,475,727 , GRCh37.p13 chr12: 100,862,529-100,869,505 NR1H4
    nsv7068612inversion1nstd229human GRCh38 chr12: 100,083,131-104,989,539 , GRCh37.p13 chr12: 100,476,909-105,383,317 EID3, RNU6-1068P, 84 more genes
    nsv7064494inversion1nstd229human GRCh38 chr12: 100,468,771-100,478,583 , GRCh37.p13 chr12: 100,862,549-100,872,361 NR1H4
    nsv7063051inversion1nstd229human GRCh38 chr12: 100,475,723-100,478,570 , GRCh37.p13 chr12: 100,869,501-100,872,348 NR1H4
    nsv6937247copy number variation1nstd229human GRCh38 chr12: 100,513,831-100,513,872 , GRCh37.p13 chr12: 100,907,609-100,907,650 NR1H4
    nsv6936470copy number variation1nstd229human GRCh38 chr12: 100,486,471-100,651,323 , GRCh37.p13 chr12: 100,880,249-101,045,101 NR1H4, GAS2L3, 1 more genes
    nsv6936056copy number variation1nstd229human GRCh38 chr12: 100,536,125-100,536,162 , GRCh37.p13 chr12: 100,929,903-100,929,940 NR1H4
    nsv6933966copy number variation1nstd229human GRCh38 chr12: 100,540,801-100,550,700 , GRCh37.p13 chr12: 100,934,579-100,944,478 NR1H4
    nsv6933029copy number variation1nstd229human GRCh38 chr12: 100,269,016-101,400,896 , GRCh37.p13 chr12: 100,662,794-101,794,674 PIGAP1, SCYL2, 10 more genes
    nsv6930901copy number variation1nstd229human GRCh38 chr12: 100,485,842-100,485,868 , GRCh37.p13 chr12: 100,879,620-100,879,646 NR1H4
    nsv6930355copy number variation1nstd229human GRCh38 chr12: 100,551,562-100,551,930 , GRCh37.p13 chr12: 100,945,340-100,945,708 NR1H4
    nsv6926720copy number variation1nstd229human GRCh38 chr12: 100,541,301-100,550,700 , GRCh37.p13 chr12: 100,935,079-100,944,478 NR1H4
    nsv6925564copy number variation1nstd229human GRCh38 chr12: 100,545,410-100,551,606 , GRCh37.p13 chr12: 100,939,188-100,945,384 NR1H4
    nsv6925126copy number variation1nstd229human GRCh38 chr12: 100,542,825-100,550,713 , GRCh37.p13 chr12: 100,936,603-100,944,491 NR1H4
    nsv6923850copy number variation1nstd229human GRCh38 chr12: 100,524,870-100,525,212 , GRCh37.p13 chr12: 100,918,648-100,918,990 NR1H4
    nsv6923067copy number variation1nstd229human GRCh38 chr12: 100,326,101-100,522,200 , GRCh37.p13 chr12: 100,719,879-100,915,978 NR1H4, SLC17A8, 1 more genes
    nsv6922635copy number variation1nstd229human GRCh38 chr12: 96,115,345-104,800,221 , GRCh37.p13 chr12: 96,509,123-105,193,999 RNY1P16, CHST11, 121 more genes
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