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Items: 1 to 20 of 347

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096918copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr2: 7,968,276-10,192,634 , GRCh38.p12 chr2: 7,828,145-10,052,507 ITGB1BP1, LINC00299, 37 more genes
    nsv7047848inversion1nstd229human GRCh38 chr2: 9,868,582-9,927,046 , GRCh37.p13 chr2: 10,008,711-10,067,175 TAF1B
    nsv7041767inversion1nstd229human GRCh38 chr2: 7,061,548-10,183,852 , GRCh37.p13 chr2: 7,201,679-10,323,978 LINC00298, KLF11, 52 more genes
    nsv6677649copy number variation1nstd229human GRCh38 chr2: 9,901,601-9,909,100 , GRCh37.p13 chr2: 10,041,730-10,049,229 TAF1B
    nsv6677617copy number variation1nstd229human GRCh38 chr2: 9,714,565-9,875,658 , GRCh37.p13 chr2: 9,854,694-10,015,787 LOC105373421, TAF1B, 2 more genes
    nsv6675353copy number variation1nstd229human GRCh38 chr2: 9,884,836-9,884,891 , GRCh37.p13 chr2: 10,024,965-10,025,020 TAF1B
    nsv6673215copy number variation1nstd229human GRCh38 chr2: 9,879,120-9,881,831 , GRCh37.p13 chr2: 10,019,249-10,021,960 TAF1B
    nsv6672078copy number variation1nstd229human GRCh38 chr2: 9,855,001-9,867,300 , GRCh37.p13 chr2: 9,995,130-10,007,429 TAF1B
    nsv6670936copy number variation1nstd229human GRCh38 chr2: 9,911,181-9,912,015 , GRCh37.p13 chr2: 10,051,310-10,052,144 TAF1B
    nsv6668948copy number variation1nstd229human GRCh38 chr2: 9,805,225-9,920,238 , GRCh37.p13 chr2: 9,945,354-10,060,367 TAF1B, LOC105373421
    nsv6667746copy number variation1nstd229human GRCh38 chr2: 9,906,957-9,909,920 , GRCh37.p13 chr2: 10,047,086-10,050,049 TAF1B
    nsv6666576copy number variation1nstd229human GRCh38 chr2: 6,592,339-11,769,396 , GRCh37.p13 chr2: 6,732,471-11,909,522 RN7SKP112, LOC101929861, 103 more genes
    nsv6659917copy number variation1nstd229human GRCh38 chr2: 9,922,901-9,961,500 , GRCh37.p13 chr2: 10,063,030-10,101,629 TAF1B, GRHL1, 1 more genes
    nsv6659193copy number variation1nstd229human GRCh38 chr2: 9,841,294-9,882,376 , GRCh37.p13 chr2: 9,981,423-10,022,505 TAF1B
    nsv6659192copy number variation1nstd229human GRCh38 chr2: 9,810,593-9,842,131 , GRCh37.p13 chr2: 9,950,722-9,982,260 TAF1B
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6554775inversion1nstd223human GRCh38 chr2: 9,869,424-9,869,942 , GRCh37.p13 chr2: 10,009,553-10,010,071 TAF1B
    nsv6354935copy number variation1nstd223human GRCh38 chr2: 9,714,565-9,875,658 , GRCh37.p13 chr2: 9,854,694-10,015,787 RNU4-73P, TAF1B, 2 more genes
    nsv6353836copy number variation1nstd223human GRCh38 chr2: 9,888,501-9,891,000 , GRCh37.p13 chr2: 10,028,630-10,031,129 TAF1B
    nsv6348371copy number variation1nstd223human GRCh38 chr2: 9,908,302-9,925,799 , GRCh37.p13 chr2: 10,048,431-10,065,928 TAF1B
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