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Items: 1 to 20 of 145

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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
    nsv7041767inversion1nstd229human GRCh38 chr2: 7,061,548-10,183,852 , GRCh37.p13 chr2: 7,201,679-10,323,978 LINC00298, KLF11, 52 more genes
    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
    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
    nsv6662148copy number variation1nstd229human GRCh38 chr2: 9,778,350-9,778,391 , GRCh37.p13 chr2: 9,918,479-9,918,520 LOC100996549
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    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
    nsv6344843copy number variation1nstd223human GRCh38 chr2: 9,772,023-9,795,245 , GRCh37.p13 chr2: 9,912,152-9,935,374 LOC100996549
    nsv6338188copy number variation1nstd223human GRCh38 chr2: 9,752,839-9,762,088 , GRCh37.p13 chr2: 9,892,968-9,902,217 LOC100996549
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6290643copy number variation1nstd102humanUncertain significance GRCh37 chr2: 8,935,077-15,722,794 , GRCh38.p12 chr2: 8,794,947-15,582,670 PPIAP60, LOC105373431, 95 more genes
    nsv6290363copy number variation1nstd102humanUncertain significance GRCh37 chr2: 9,717,186-12,013,065 , GRCh38.p12 chr2: 9,577,057-11,872,939 RNU4-73P, CYS1, 56 more genes
    nsv6161966copy number variation1nstd214human GRCh38 chr2: 9,766,034-9,766,100 , GRCh37.p13 chr2: 9,906,163-9,906,229 LOC100996549
    nsv6134471copy number variation1nstd213human GRCh37 chr2: 9,710,000-10,900,001 , GRCh38.p12 chr2: 9,569,871-10,759,875 HPCAL1, ODC1, 26 more genes
    nsv6134375copy number variation1nstd213human GRCh37 chr2: 9,700,000-10,940,001 , GRCh38.p12 chr2: 9,559,871-10,799,875 HPCAL1, ODC1, 28 more genes
    nsv6051384insertion1nstd212human GRCh38 chr2: 9,776,953-9,776,953 , GRCh37.p13 chr2: 9,917,082-9,917,082 LOC100996549
    nsv5963372insertion1nstd209human GRCh38 chr2: 9,776,922-9,776,922 , GRCh37.p13 chr2: 9,917,051-9,917,051 LOC100996549
    nsv5834470copy number variation1nstd209human GRCh38 chr2: 9,764,653-9,767,400 , GRCh37.p13 chr2: 9,904,782-9,907,529 LOC100996549
    nsv5834157copy number variation1nstd209human GRCh38 chr2: 9,737,802-9,763,402 , GRCh37.p13 chr2: 9,877,931-9,903,531 RNU4-73P, LOC100996549
    nsv5614009insertion1nstd207human GRCh38 chr2: 9,776,953-9,776,953 , GRCh37.p13 chr2: 9,917,082-9,917,082 LOC100996549
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