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Items: 1 to 20 of 239

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077246inversion1nstd229human GRCh38 chr15: 64,487,767-67,498,498 , GRCh37.p13 chr15: 64,779,966-67,790,836 LETM1P1, MIR4512, 74 more genes
    nsv7069168inversion1nstd229human GRCh38 chr15: 65,085,774-67,006,275 , GRCh37.p13 chr15: 65,378,112-67,298,613 MEGF11, HNRNPA1P44, 51 more genes
    nsv7063733inversion1nstd229human GRCh38 chr15: 63,479,684-65,571,065 , GRCh37.p13 chr15: 63,771,883-65,863,403 TRIP4, RNU5B-1, 45 more genes
    nsv6976656copy number variation1nstd229human GRCh38 chr15: 65,330,429-65,388,121 , GRCh37.p13 chr15: 65,622,767-65,680,459 IGDCC3, IGDCC4
    nsv6974022copy number variation1nstd229human GRCh38 chr15: 65,326,077-65,326,476 , GRCh37.p13 chr15: 65,618,415-65,618,814 IGDCC3
    nsv6973999copy number variation1nstd229human GRCh38 chr15: 65,250,272-65,345,734 , GRCh37.p13 chr15: 65,542,610-65,638,072 IGDCC3, RNU5B-1, 3 more genes
    nsv6973902copy number variation1nstd229human GRCh38 chr15: 65,370,095-65,370,252 , GRCh37.p13 chr15: 65,662,433-65,662,590 IGDCC3
    nsv6968314copy number variation1nstd229human GRCh38 chr15: 65,340,636-65,377,101 , GRCh37.p13 chr15: 65,632,974-65,669,439 IGDCC3
    nsv6637712copy number variation1nstd102humanUncertain significance GRCh37 chr15: 65,437,410-65,659,163 , GRCh38.p12 chr15: 65,145,072-65,366,825 RNU5A-1, CILP, 6 more genes
    nsv6623277copy number variation1nstd224human GRCh37 chr15: 65,622,889-65,678,901 , GRCh38.p12 chr15: 65,330,551-65,386,563 IGDCC3, IGDCC4
    nsv6513890copy number variation1nstd223human GRCh38 chr15: 65,354,701-65,356,600 , GRCh37.p13 chr15: 65,647,039-65,648,938 IGDCC3
    nsv6511083copy number variation1nstd223human GRCh38 chr15: 65,345,237-65,346,287 , GRCh37.p13 chr15: 65,637,575-65,638,625 IGDCC3
    nsv6499841copy number variation1nstd223human GRCh38 chr15: 65,326,077-65,326,473 , GRCh37.p13 chr15: 65,618,415-65,618,811 IGDCC3
    nsv6314072copy number variation1nstd102humanUncertain significance GRCh37 chr15: 64,978,681-65,679,053 , GRCh38.p12 chr15: 64,686,482-65,386,715 CLPX, RNU5B-1, 22 more genes
    nsv6133150copy number variation1nstd213human GRCh37 chr15: 59,870,000-66,270,001 , GRCh38.p12 chr15: 59,577,801-65,977,663 GTF2A2, OAZ2, 115 more genes
    nsv5968048insertion1nstd209human GRCh38 chr15: 65,356,834-65,356,834 , GRCh37.p13 chr15: 65,649,172-65,649,172 IGDCC3
    nsv5941129copy number variation1nstd209human GRCh38 chr15: 65,326,077-65,326,472 , GRCh37.p13 chr15: 65,618,415-65,618,810 IGDCC3
    nsv5940912copy number variation1nstd209human GRCh38 chr15: 65,345,237-65,346,286 , GRCh37.p13 chr15: 65,637,575-65,638,624 IGDCC3
    nsv5599853copy number variation1nstd207human GRCh38 chr15: 65,345,237-65,346,286 , GRCh37.p13 chr15: 65,637,575-65,638,624 IGDCC3
    nsv5597180copy number variation1nstd207human GRCh38 chr15: 65,326,077-65,326,472 , GRCh37.p13 chr15: 65,618,415-65,618,810 IGDCC3
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