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Items: 1 to 20 of 942

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098791copy number variation1nstd102humanPathogenic GRCh37 chr17: 55,442,363-56,309,063 , GRCh38.p12 chr17: 57,365,002-58,231,702 MKS1, OR4D2, 21 more genes
    nsv7065613inversion1nstd229human GRCh38 chr17: 57,293,594-57,296,682 , GRCh37.p13 chr17: 55,370,955-55,374,043 MSI2
    nsv7060590inversion1nstd229human GRCh38 chr17: 57,278,413-57,285,618 , GRCh37.p13 chr17: 55,355,774-55,362,979 MSI2
    nsv7059350inversion1nstd229human GRCh38 chr17: 57,297,775-57,299,543 , GRCh37.p13 chr17: 55,375,136-55,376,904 MSI2
    nsv7058620inversion1nstd229human GRCh38 chr17: 57,249,365-57,569,630 , GRCh37.p13 chr17: 55,326,726-55,646,991 LOC101927557, MSI2, 2 more genes
    nsv6998015copy number variation1nstd229human GRCh38 chr17: 57,374,101-57,377,800 , GRCh37.p13 chr17: 55,451,462-55,455,161 MSI2
    nsv6994841copy number variation1nstd229human GRCh38 chr17: 57,505,565-57,512,190 , GRCh37.p13 chr17: 55,582,926-55,589,551 MSI2
    nsv6994687copy number variation1nstd229human GRCh38 chr17: 57,459,174-57,469,483 , GRCh37.p13 chr17: 55,536,535-55,546,844 MSI2
    nsv6994267copy number variation1nstd229human GRCh38 chr17: 57,512,501-57,525,400 , GRCh37.p13 chr17: 55,589,862-55,602,761 MSI2, LOC101927557
    nsv6993806copy number variation1nstd229human GRCh38 chr17: 57,337,545-57,340,647 , GRCh37.p13 chr17: 55,414,906-55,418,008 MSI2
    nsv6992810copy number variation1nstd229human GRCh38 chr17: 57,620,053-57,620,202 , GRCh37.p13 chr17: 55,697,414-55,697,563 MSI2
    nsv6992365copy number variation1nstd229human GRCh38 chr17: 57,464,355-57,465,422 , GRCh37.p13 chr17: 55,541,716-55,542,783 MSI2
    nsv6992327copy number variation1nstd229human GRCh38 chr17: 57,374,530-57,377,830 , GRCh37.p13 chr17: 55,451,891-55,455,191 MSI2
    nsv6991954copy number variation1nstd229human GRCh38 chr17: 57,509,566-57,510,363 , GRCh37.p13 chr17: 55,586,927-55,587,724 MSI2
    nsv6991691copy number variation1nstd229human GRCh38 chr17: 57,339,365-57,357,611 , GRCh37.p13 chr17: 55,416,726-55,434,972 MSI2
    nsv6991519copy number variation1nstd229human GRCh38 chr17: 57,452,955-57,479,588 , GRCh37.p13 chr17: 55,530,316-55,556,949 MSI2
    nsv6991205copy number variation1nstd229human GRCh38 chr17: 57,656,393-57,663,798 , GRCh37.p13 chr17: 55,733,754-55,741,159 MSI2
    nsv6990927copy number variation1nstd229human GRCh38 chr17: 57,610,450-57,612,556 , GRCh37.p13 chr17: 55,687,811-55,689,917 MSI2
    nsv6990536copy number variation1nstd229human GRCh38 chr17: 57,437,712-57,437,822 , GRCh37.p13 chr17: 55,515,073-55,515,183 MSI2
    nsv6990032copy number variation1nstd229human GRCh38 chr17: 57,493,927-57,499,922 , GRCh37.p13 chr17: 55,571,288-55,577,283 MSI2
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