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Items: 1 to 20 of 369

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5940125copy number variation1nstd209human GRCh38 chr15: 34,904,642-34,905,657 , GRCh37.p13 chr15: 35,196,843-35,197,858 AQR
    nsv5932782copy number variation1nstd209human GRCh38 chr15: 34,920,819-34,926,046 , GRCh37.p13 chr15: 35,213,020-35,218,247 AQR
    nsv5853565copy number variation1nstd209human GRCh38 chr15: 34,920,811-34,925,992 , GRCh37.p13 chr15: 35,213,012-35,218,193 AQR
    nsv5852919copy number variation1nstd209human GRCh38 chr15: 34,904,683-34,905,706 , GRCh37.p13 chr15: 35,196,884-35,197,907 AQR
    nsv5709434mobile element insertion1nstd211human GRCh38 chr15: 34,930,849-34,930,849 , GRCh37.p13 chr15: 35,223,050-35,223,050 AQR
    nsv5505915copy number variation1nstd206human GRCh38 chr15: 34,940,957-34,978,469 , GRCh37.p13 chr15: 35,233,158-35,270,670 AQR, RPL36AP8, 1 more genes
    nsv5503914copy number variation1nstd206human GRCh38 chr15: 34,895,014-34,895,224 , GRCh37.p13 chr15: 35,187,215-35,187,425 AQR
    nsv5501032copy number variation1nstd206human GRCh38 chr15: 34,904,643-34,905,658 , GRCh37.p13 chr15: 35,196,844-35,197,859 AQR
    nsv5496825copy number variation1nstd206human GRCh38 chr15: 34,890,726-34,891,020 , GRCh37.p13 chr15: 35,182,927-35,183,221 AQR
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5357796translocation1nstd200human GRCh38 chr15: 34,905,658-34,905,658 , GRCh38 chr15: 34,904,643-34,904,643 , GRCh37.p13 chr15: 35,196,844-35,196,844 , GRCh37.p13 chr15: 35,197,859-35,197,859 AQR
    nsv5357794translocation1nstd200human GRCh38 chr15: 34,895,217-34,895,217 , GRCh38 chr15: 34,894,686-34,894,686 , GRCh37.p13 chr15: 35,186,887-35,186,887 , GRCh37.p13 chr15: 35,187,418-35,187,418 AQR
    nsv5312575copy number variation1nstd204human GRCh38.p13 chr15: 34,856,308-34,858,063 , GRCh37.p13 chr15: 35,148,509-35,150,264 AQR
    nsv5304138copy number variation1nstd204human GRCh38.p13 chr15: 34,904,639-34,905,659 , GRCh37.p13 chr15: 35,196,840-35,197,860 AQR
    nsv5215508mobile element deletion1nstd204human GRCh38.p13 chr15: 34,966,862-34,967,200 , GRCh37.p13 chr15: 35,259,063-35,259,401 AQR
    nsv5199412mobile element insertion1nstd203human GRCh38 chr15: 34,947,513-34,947,539 , GRCh37.p13 chr15: 35,239,714-35,239,740 AQR
    nsv5195657mobile element insertion1nstd203human GRCh38 chr15: 34,947,507-34,947,541 , GRCh37.p13 chr15: 35,239,708-35,239,742 AQR
    nsv5192418mobile element insertion1nstd203human GRCh38 chr15: 34,943,844-34,943,858 , GRCh37.p13 chr15: 35,236,045-35,236,059 RPL36AP8, AQR
    nsv5159062mobile element insertion1nstd203human GRCh38 chr15: 34,895,159-34,895,188 , GRCh37.p13 chr15: 35,187,360-35,187,389 AQR
    nsv5158569mobile element insertion1nstd203human GRCh38 chr15: 34,895,160-34,895,206 , GRCh37.p13 chr15: 35,187,361-35,187,407 AQR
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