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Items: 1 to 20 of 194

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146857insertion1nstd232human GRCh37.p13 chr6: 83,898,519-83,898,519 , GRCh38.p12 chr6: 83,188,800-83,188,800 PGM3
    nsv7098884copy number variation1nstd102humanPathogenic GRCh37 chr6: 82,828,591-86,578,811 , GRCh38.p12 chr6: 82,118,874-85,869,093 LOC105377879, LOC100421583, 47 more genes
    nsv6815298copy number variation1nstd229human GRCh38 chr6: 83,150,513-83,155,022 , GRCh37.p13 chr6: 83,860,232-83,864,741 DOP1A, PGM3
    nsv6811934copy number variation1nstd229human GRCh38 chr6: 83,173,385-83,173,897 , GRCh37.p13 chr6: 83,883,104-83,883,616 PGM3
    nsv6806693copy number variation1nstd229human GRCh38 chr6: 83,069,562-83,169,205 , GRCh37.p13 chr6: 83,779,281-83,878,924 DOP1A, PGM3
    nsv6804840copy number variation1nstd229human GRCh38 chr6: 83,175,455-83,175,629 , GRCh37.p13 chr6: 83,885,174-83,885,348 PGM3
    nsv6799121copy number variation1nstd229human GRCh38 chr6: 83,176,393-83,180,559 , GRCh37.p13 chr6: 83,886,112-83,890,278 PGM3
    nsv6791212copy number variation1nstd229human GRCh38 chr6: 77,944,413-86,852,671 , GRCh37.p13 chr6: 78,654,130-87,562,389 SH3BGRL2, LCAL1, 93 more genes
    nsv6636874copy number variation1nstd102humanUncertain significance GRCh37 chr6: 81,087,736-84,200,632 , GRCh38.p12 chr6: 80,378,019-83,490,913 PGM3, ME1, 24 more genes
    nsv6634392copy number variation1nstd102humanUncertain significance GRCh37 chr6: 78,911,022-98,909,173 , GRCh38.p12 chr6: 78,201,305-98,461,297 MTHFD2P2, RPL7P27, 212 more genes
    nsv6631462copy number variation1nstd224human GRCh37 chr6: 83,252,450-83,872,643 , GRCh38.p12 chr6: 82,542,733-83,162,924 PGM3, DOP1A, 4 more genes
    nsv6558068inversion1nstd223human GRCh38 chr6: 83,171,663-83,172,642 , GRCh37.p13 chr6: 83,881,382-83,882,361 DOP1A, PGM3
    nsv6405981copy number variation1nstd223human GRCh38 chr6: 83,191,902-83,192,327 , GRCh37.p13 chr6: 83,901,621-83,902,046 PGM3, RWDD2A
    nsv6403949copy number variation1nstd223human GRCh38 chr6: 83,176,392-83,180,558 , GRCh37.p13 chr6: 83,886,111-83,890,277 PGM3
    nsv6402520copy number variation1nstd223human GRCh38 chr6: 83,173,464-83,173,992 , GRCh37.p13 chr6: 83,883,183-83,883,711 PGM3
    nsv6399260copy number variation1nstd223human GRCh38 chr6: 83,108,063-83,419,637 , GRCh37.p13 chr6: 83,817,782-84,129,356 ME1, PGM3, 2 more genes
    nsv6314506complex chromosomal rearrangement7nstd102humanUncertain significance GRCh37 chr6: 21,715,677-21,715,677 , GRCh37 chr6: 21,715,677-21,715,677 , GRCh37 chr6: 83,891,695-83,891,695 , GRCh37 chr6: 123,834,806-123,834,806 , GRCh37 chr6: 78,967,194-78,967,194 , GRCh37 chr6: 79,036,476-79,036,476 , GRCh37 chr6: 123,834,803-123,834,803 , GRCh37 chr6: 83,891,695-83,891,695 , GRCh37 chr6: 127,919,515-127,919,515 , GRCh37 chr6: 128,030,235-128,030,235 , GRCh37 chr6: 84,496,838-84,496,838 , GRCh37 chr6: 84,496,838-84,496,838 , GRCh37 chr13: 57,178,494-57,178,494 , GRCh37 chr13: 57,178,506-57,178,506 , GRCh38.p12 chr6: 78,257,477-78,257,477 , GRCh38.p12 chr6: 78,326,759-78,326,759 , GRCh38.p12 chr6: 83,181,976-83,181,976 , GRCh38.p12 chr6: 83,787,119-83,787,119 , GRCh38.p12 chr6: 123,513,661-123,513,661 , GRCh38.p12 chr6: 21,715,446-21,715,446 , GRCh38.p12 chr6: 21,715,446-21,715,446 , GRCh38.p12 chr6: 127,598,370-127,598,370 , GRCh38.p12 chr6: 127,709,090-127,709,090 , GRCh38.p12 chr6: 83,181,976-83,181,976 , GRCh38.p12 chr6: 83,787,119-83,787,119 , GRCh38.p12 chr6: 123,513,658-123,513,658 , GRCh38.p12 chr13: 56,604,360-56,604,360 , GRCh38.p12 chr13: 56,604,372-56,604,372 , GRCh38.p12 chr6|NT_187556.1: 54,288-54,288 CASC15, PGM3, 5 more genes
    nsv6313857copy number variation1nstd102humanPathogenic GRCh37 chr6: 69,938,252-94,379,210 , GRCh38.p12 chr6: 69,228,360-93,669,492 LOC101928570, RNU4-72P, 288 more genes
    nsv6313843copy number variation1nstd102humanUncertain significance GRCh37 chr6: 83,888,683-83,941,662 , GRCh38.p12 chr6: 83,178,964-83,231,943 RWDD2A, PGM3, 1 more genes
    nsv6312070copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr6: 83,878,953-83,900,987 , GRCh38.p12 chr6: 83,169,234-83,191,268 PGM3, DOP1A
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