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Items: 1 to 20 of 312

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130815insertion1nstd186human GRCh37 chr22: 39,009,429-39,009,470 , GRCh38.p12 chr22: 38,613,424-38,613,465 FAM227A
    nsv6124622copy number variation1nstd186human GRCh37 chr22: 39,044,049-39,044,692 , GRCh38.p12 chr22: 38,648,044-38,648,687 FAM227A
    nsv5967207copy number variation1nstd209human GRCh38 chr22: 38,645,141-38,648,356 , GRCh37.p13 chr22: 39,041,146-39,044,361 FAM227A
    nsv5963133copy number variation1nstd209human GRCh38 chr22: 38,613,082-38,613,138 , GRCh37.p13 chr22: 39,009,087-39,009,143 FAM227A
    nsv5957921copy number variation1nstd209human GRCh38 chr22: 38,581,652-38,585,850 , GRCh37.p13 chr22: 38,977,657-38,981,855 FAM227A
    nsv5956836copy number variation1nstd209human GRCh38 chr22: 38,644,341-38,644,435 , GRCh37.p13 chr22: 39,040,346-39,040,440 FAM227A
    nsv5884739copy number variation1nstd209human GRCh38 chr22: 38,581,838-38,583,137 , GRCh37.p13 chr22: 38,977,843-38,979,142 FAM227A
    nsv5879624copy number variation1nstd209human GRCh38 chr22: 38,645,091-38,648,480 , GRCh37.p13 chr22: 39,041,096-39,044,485 FAM227A
    nsv5867673copy number variation1nstd209human GRCh38 chr22: 38,581,638-38,585,899 , GRCh37.p13 chr22: 38,977,643-38,981,904 FAM227A
    nsv5672240insertion1nstd207human GRCh38 chr22: 38,644,446-38,644,446 , GRCh37.p13 chr22: 39,040,451-39,040,451 FAM227A
    nsv5670152insertion1nstd207human GRCh38 chr22: 38,644,315-38,644,315 , GRCh37.p13 chr22: 39,040,320-39,040,320 FAM227A
    nsv5669051insertion1nstd207human GRCh38 chr22: 38,613,414-38,613,414 , GRCh37.p13 chr22: 39,009,419-39,009,419 FAM227A
    nsv5667166insertion1nstd207human GRCh38 chr22: 38,613,116-38,613,116 , GRCh37.p13 chr22: 39,009,121-39,009,121 FAM227A
    nsv5665951insertion1nstd207human GRCh38 chr22: 38,629,645-38,629,645 , GRCh37.p13 chr22: 39,025,650-39,025,650 FAM227A
    nsv5604329copy number variation1nstd207human GRCh38 chr22: 38,629,645-38,629,701 , GRCh37.p13 chr22: 39,025,650-39,025,706 FAM227A
    nsv5598439copy number variation1nstd207human GRCh38 chr22: 38,648,357-38,648,721 , GRCh37.p13 chr22: 39,044,362-39,044,726 FAM227A
    nsv5552064insertion1nstd206human GRCh38 chr22: 38,613,424-38,613,465 , GRCh37.p13 chr22: 39,009,429-39,009,470 FAM227A
    nsv5542622copy number variation1nstd206human GRCh38 chr22: 38,643,938-38,645,252 , GRCh37.p13 chr22: 39,039,943-39,041,257 FAM227A
    nsv5541254copy number variation1nstd206human GRCh38 chr22: 38,625,731-38,627,305 , GRCh37.p13 chr22: 39,021,736-39,023,310 FAM227A
    nsv5539967copy number variation1nstd206human GRCh38 chr22: 38,622,504-38,625,115 , GRCh37.p13 chr22: 39,018,509-39,021,120 FAM227A
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