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Items: 1 to 20 of 1151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142554copy number variation1nstd232human GRCh37.p13 chr16: 25,721,774-25,721,828 , GRCh38.p12 chr16: 25,710,453-25,710,507 HS3ST4
    nsv7137115copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,467,726-29,044,717 , GRCh38.p12 chr16: 21,456,405-29,033,396 OTOAP1, GGA2, 148 more genes
    nsv7077320inversion1nstd229human GRCh38 chr16: 25,922,037-25,975,757 , GRCh37.p13 chr16: 25,933,358-25,987,078 HS3ST4
    nsv7074824inversion1nstd229human GRCh38 chr16: 25,922,046-25,925,072 , GRCh37.p13 chr16: 25,933,367-25,936,393 HS3ST4
    nsv7072180inversion1nstd229human GRCh38 chr16: 25,741,699-25,745,288 , GRCh37.p13 chr16: 25,753,020-25,756,609 HS3ST4
    nsv7061426inversion1nstd229human GRCh38 chr16: 25,833,461-25,836,940 , GRCh37.p13 chr16: 25,844,782-25,848,261 HS3ST4
    nsv7058198inversion1nstd229human GRCh38 chr16: 26,083,732-26,083,854 , GRCh37.p13 chr16: 26,095,053-26,095,175 HS3ST4
    nsv6997753copy number variation1nstd229human GRCh38 chr16: 25,892,525-25,892,730 , GRCh37.p13 chr16: 25,903,846-25,904,051 HS3ST4
    nsv6997746copy number variation1nstd229human GRCh38 chr16: 25,942,060-25,954,213 , GRCh37.p13 chr16: 25,953,381-25,965,534 HS3ST4
    nsv6997085copy number variation1nstd229human GRCh38 chr16: 26,107,901-26,141,900 , GRCh37.p13 chr16: 26,119,222-26,153,221 HS3ST4
    nsv6997000copy number variation1nstd229human GRCh38 chr16: 25,916,651-25,936,062 , GRCh37.p13 chr16: 25,927,972-25,947,383 HS3ST4
    nsv6996677copy number variation1nstd229human GRCh38 chr16: 25,869,100-25,872,966 , GRCh37.p13 chr16: 25,880,421-25,884,287 HS3ST4
    nsv6995836copy number variation1nstd229human GRCh38 chr16: 26,107,100-26,109,624 , GRCh37.p13 chr16: 26,118,421-26,120,945 HS3ST4
    nsv6994049copy number variation1nstd229human GRCh38 chr16: 26,052,479-26,052,614 , GRCh37.p13 chr16: 26,063,800-26,063,935 HS3ST4
    nsv6993007copy number variation1nstd229human GRCh38 chr16: 25,866,783-25,866,828 , GRCh37.p13 chr16: 25,878,104-25,878,149 HS3ST4
    nsv6991997copy number variation1nstd229human GRCh38 chr16: 25,823,532-25,826,228 , GRCh37.p13 chr16: 25,834,853-25,837,549 HS3ST4, LOC100420641
    nsv6991546copy number variation1nstd229human GRCh38 chr16: 25,873,322-25,873,378 , GRCh37.p13 chr16: 25,884,643-25,884,699 HS3ST4
    nsv6991396copy number variation1nstd229human GRCh38 chr16: 25,723,301-25,727,000 , GRCh37.p13 chr16: 25,734,622-25,738,321 HS3ST4
    nsv6988767copy number variation1nstd229human GRCh38 chr16: 25,754,367-25,756,662 , GRCh37.p13 chr16: 25,765,688-25,767,983 HS3ST4
    nsv6988183copy number variation1nstd229human GRCh38 chr16: 25,814,320-25,824,460 , GRCh37.p13 chr16: 25,825,641-25,835,781 HS3ST4, LOC100420641
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