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Items: 1 to 20 of 206

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5937953copy number variation1nstd209human GRCh38 chr17: 81,371,208-81,374,250 , GRCh37.p13 chr17: 79,345,008-79,348,050 , GRCh37.p13 chr17|NW_003871087.1: 25,846-28,888 LINC03048
    nsv5518679copy number variation1nstd206human GRCh38 chr17: 81,361,197-81,377,388 , GRCh37.p13 chr17: 79,334,997-79,351,188 , GRCh37.p13 chr17|NW_003871087.1: 15,835-32,026 LINC03048
    nsv5298108copy number variation1nstd204human GRCh38.p13 chr17: 80,930,501-82,586,000 , GRCh37.p13 chr17: 78,904,301-80,543,876 , PPP1R27, 89 more genes
    nsv5294695copy number variation1nstd204human GRCh38.p13 chr17: 80,930,501-81,587,000 , GRCh37.p13 chr17: 78,904,301-79,554,026 , LOC105371926, 32 more genes
    nsv5014108copy number variation1nstd200human GRCh38 chr17: 81,203,730-81,483,549 , GRCh37.p13 chr17: 79,177,530-79,319,162 , LINC03048, 13 more genes
    nsv4867515copy number variation1nstd200human GRCh37 chr17: 79,344,951-79,347,987 , GRCh38.p12 chr17: 81,371,151-81,374,187 LINC03048
    nsv4867514copy number variation1nstd200human GRCh37 chr17: 79,335,037-79,351,109 , GRCh38.p12 chr17: 81,361,237-81,377,309 LINC03048
    nsv4625921copy number variation1nstd183human GRCh37 chr17: 78,632,841-79,703,517 , GRCh38.p12 chr17: 80,659,041-81,736,487 , HGS, 44 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv4457483copy number variation1nstd102humanPathogenic GRCh37 chr17: 78,608,912-81,041,938 , GRCh38.p12 chr17: 80,635,112-83,084,062 HEXD, LOC105371929, 94 more genes
    nsv4374349copy number variation1nstd173human GRCh37 chr17: 79,330,617-80,189,678 , GRCh38.p12 chr17: 81,356,817-82,231,802 , FAAP100, 49 more genes
    nsv4267141copy number variation1nstd166human GRCh37.p13 chr17: 79,329,634-79,410,419 , GRCh38.p12 chr17: 81,355,834-81,443,393 LINC03048, MIR4740, 1 more genes
    nsv4262869copy number variation1nstd166human GRCh37.p13 chr17: 79,260,089-79,398,035 , GRCh38.p12 chr17: 81,286,289-81,424,235 , BAHCC1, 5 more genes
    nsv4259231copy number variation1nstd166human GRCh37.p13 chr17: 79,335,068-79,351,148 , GRCh38.p12 chr17: 81,361,268-81,377,348 LINC03048
    nsv3965354insertion1nstd168human GRCh38 chr17: 81,184,403-81,452,333 , GRCh37.p13 chr17: 79,158,203-79,319,162 , CEP131, 11 more genes
    nsv3919635copy number variation1nstd102humanPathogenic GRCh37 chr17: 76,088,317-81,044,553 , NCBI36 chr17: 73,599,912-78,637,842 , GRCh38 chr17: 78,092,236-83,086,677 LINC03048, MIR3186, 154 more genes
    nsv3919156copy number variation1nstd102humanPathogenic GRCh38 chr17: 69,916,435-83,102,552 , GRCh37 chr17: 67,912,576-81,048,189 , NCBI36 chr17: 65,424,171-78,653,717 CD300A, RNF213, 359 more genes
    nsv3917654copy number variation1nstd102humanPathogenic NCBI36 chr17: 64,716,815-78,637,842 , GRCh37 chr17: 67,205,220-81,044,553 , GRCh38 chr17: 69,209,079-83,086,677 LOC101928447, GRB2, 368 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 LOC105371922, GJD3, 1855 more genes
    nsv3914738copy number variation1nstd102humanPathogenic NCBI36 chr17: 74,409,636-78,637,842 , GRCh37 chr17: 76,898,041-81,044,553 , GRCh38 chr17: 78,901,959-83,086,677 MIR338, DUS1L, 127 more genes
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