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Items: 1 to 20 of 425

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095172copy number variation1nstd102humanUncertain significance GRCh37 chr17: 56,798,087-57,771,213 , GRCh38.p12 chr17: 58,720,726-59,693,852 LINC01476, RNU2-58P, 22 more genes
    nsv7074808inversion1nstd229human GRCh38 chr17: 59,254,307-59,555,888 , GRCh37.p13 chr17: 57,331,668-57,633,249 LINC01476, YPEL2, 6 more genes
    nsv7070986inversion1nstd229human GRCh38 chr17: 59,331,393-62,738,993 , GRCh37.p13 chr17: 57,408,754-60,816,354 MIR21, LINC01476, 83 more genes
    nsv7069096inversion1nstd229human GRCh38 chr17: 59,258,055-59,498,553 , GRCh37.p13 chr17: 57,335,416-57,575,914 LOC105371845, YPEL2, 4 more genes
    nsv7065863inversion1nstd229human GRCh38 chr17: 59,173,715-59,455,273 , GRCh37.p13 chr17: 57,251,076-57,532,634 PRR11, GDPD1, 6 more genes
    nsv7064893inversion1nstd229human GRCh38 chr17: 59,497,993-59,509,636 , GRCh37.p13 chr17: 57,575,354-57,586,997 LOC105371845, LINC01476
    nsv7062151inversion1nstd229human GRCh38 chr17: 58,705,434-61,610,111 , GRCh37.p13 chr17: 56,782,795-59,687,472 RNU4-13P, LOC105371850, 74 more genes
    nsv7060153inversion1nstd229human GRCh38 chr17: 59,254,088-59,444,835 , GRCh37.p13 chr17: 57,331,449-57,522,196 YPEL2, MIR4729, 3 more genes
    nsv7059487inversion1nstd229human GRCh38 chr17: 59,499,603-59,510,647 , GRCh37.p13 chr17: 57,576,964-57,588,008 LOC105371845, LINC01476
    nsv7059382inversion1nstd229human GRCh38 chr17: 59,393,521-59,501,560 , GRCh37.p13 chr17: 57,470,882-57,578,921 LINC01476, LOC105371845, 1 more genes
    nsv6997058copy number variation1nstd229human GRCh38 chr17: 59,447,560-59,454,230 , GRCh37.p13 chr17: 57,524,921-57,531,591 LINC01476
    nsv6996573copy number variation1nstd229human GRCh38 chr17: 59,500,645-59,510,315 , GRCh37.p13 chr17: 57,578,006-57,587,676 LINC01476, LOC105371845
    nsv6995972copy number variation1nstd229human GRCh38 chr17: 59,379,001-59,457,800 , GRCh37.p13 chr17: 57,456,362-57,535,161 LINC01476, YPEL2
    nsv6995425copy number variation1nstd229human GRCh38 chr17: 59,359,070-59,445,571 , GRCh37.p13 chr17: 57,436,431-57,522,932 YPEL2, LINC01476, 1 more genes
    nsv6995393copy number variation1nstd229human GRCh38 chr17: 59,513,701-59,517,300 , GRCh37.p13 chr17: 57,591,062-57,594,661 LINC01476
    nsv6993631copy number variation1nstd229human GRCh38 chr17: 59,526,655-59,528,774 , GRCh37.p13 chr17: 57,604,016-57,606,135 LOC105371847, LINC01476
    nsv6992443copy number variation1nstd229human GRCh38 chr17: 59,074,120-59,569,948 , GRCh37.p13 chr17: 57,151,481-57,647,309 GDPD1, YPEL2, 15 more genes
    nsv6991319copy number variation1nstd229human GRCh38 chr17: 59,444,627-59,450,218 , GRCh37.p13 chr17: 57,521,988-57,527,579 LINC01476
    nsv6991155copy number variation1nstd229human GRCh38 chr17: 59,498,249-59,502,337 , GRCh37.p13 chr17: 57,575,610-57,579,698 LOC105371845, LINC01476
    nsv6989297copy number variation1nstd229human GRCh38 chr17: 59,462,586-59,467,584 , GRCh37.p13 chr17: 57,539,947-57,544,945 LINC01476
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