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Items: 1 to 20 of 133

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905518copy number variation1nstd209human GRCh38 chr6: 150,322,298-150,326,704 , GRCh37.p13 chr6: 150,643,434-150,647,840 RNU4-7P
    nsv5844124copy number variation1nstd209human GRCh38 chr6: 150,322,297-150,326,671 , GRCh37.p13 chr6: 150,643,433-150,647,807 RNU4-7P
    nsv5583522copy number variation1nstd207human GRCh38 chr6: 150,322,298-150,326,704 , GRCh37.p13 chr6: 150,643,434-150,647,840 RNU4-7P
    nsv5464057copy number variation1nstd206human GRCh38 chr6: 150,322,298-150,326,705 , GRCh37.p13 chr6: 150,643,434-150,647,841 RNU4-7P
    nsv5310859copy number variation1nstd204human GRCh38.p13 chr6: 150,322,288-150,326,714 , GRCh37.p13 chr6: 150,643,424-150,647,850 RNU4-7P
    nsv5309860copy number variation1nstd204human GRCh37.p13 chr6: 150,482,738-151,022,419 , GRCh38.p13 chr6: 150,161,602-150,701,283 RNU4-7P, PLEKHG1, 5 more genes
    nsv5233960copy number variation1nstd204human GRCh38.p13 chr6: 150,322,222-150,326,521 , GRCh37.p13 chr6: 150,643,358-150,647,657 RNU4-7P
    nsv5226443copy number variation1nstd204human GRCh37.p13 chr6: 150,482,837-151,022,136 , GRCh38.p13 chr6: 150,161,701-150,701,000 RNU4-7P, PLEKHG1, 5 more genes
    nsv4943370copy number variation1nstd200human GRCh38 chr6: 150,322,298-150,326,705 , GRCh37.p13 chr6: 150,643,434-150,647,841 RNU4-7P
    nsv4810893copy number variation1nstd200human GRCh37 chr6: 150,643,434-150,647,841 , GRCh38.p12 chr6: 150,322,298-150,326,705 RNU4-7P
    nsv4675234copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,431,322-154,120,064 , GRCh38.p12 chr6: 149,110,186-153,798,929 RNU7-3P, HSPD1P16, 86 more genes
    nsv4659105copy number variation1nstd186human GRCh37 chr6: 150,643,454-150,647,802 , GRCh38.p12 chr6: 150,322,318-150,326,666 RNU4-7P
    nsv4658074copy number variation1nstd186human GRCh37 chr6: 150,643,434-150,647,841 , GRCh38.p12 chr6: 150,322,298-150,326,705 RNU4-7P
    nsv4643906copy number variation4nstd186human GRCh37 chr6: 150,643,434-150,647,841 , GRCh38.p12 chr6: 150,322,298-150,326,705 RNU4-7P
    nsv4636987copy number variation1nstd186human GRCh37 chr6: 150,643,428-150,647,846 , GRCh38.p12 chr6: 150,322,292-150,326,710 RNU4-7P
    nsv4617890copy number variation1nstd183human GRCh37 chr6: 150,643,454-150,647,750 , GRCh38.p12 chr6: 150,322,318-150,326,614 RNU4-7P
    nsv4617756copy number variation1nstd183human GRCh37 chr6: 150,643,434-150,647,841 , GRCh38.p12 chr6: 150,322,298-150,326,705 RNU4-7P
    nsv4613502copy number variation1nstd183human GRCh37 chr6: 150,643,454-150,647,802 , GRCh38.p12 chr6: 150,322,318-150,326,666 RNU4-7P
    nsv4456488copy number variation1nstd102humanPathogenic GRCh37 chr6: 148,195,086-160,127,254 , GRCh38.p12 chr6: 147,873,950-159,706,222 PDCL3P5, SYTL3, 176 more genes
    nsv4406522copy number variation1nstd174human GRCh37 chr6: 150,643,428-150,647,846 , GRCh38.p12 chr6: 150,322,292-150,326,710 RNU4-7P
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