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Items: 1 to 20 of 186

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5017044copy number variation1nstd200human GRCh38 chr17: 81,441,456-81,816,579 , GRCh37.p13 chr17: 79,498,418-79,774,455 , LOC105376789, 19 more genes
    nsv4633211copy number variation1nstd183human GRCh37 chr17: 79,376,011-79,478,019 , GRCh38.p12 chr17: 81,402,211-81,510,993 , ACTG1, 4 more genes
    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
    nsv4267155copy number variation1nstd166human GRCh37.p13 chr17: 79,477,861-79,477,952 , GRCh38.p12 chr17: 81,510,835-81,510,926 ACTG1
    nsv4264413copy number variation1nstd166human GRCh37.p13 chr17: 79,478,000-79,483,000 , GRCh38.p12 chr17: 81,510,974-81,515,974 FSCN2, ACTG1
    nsv4256561copy number variation1nstd166human GRCh37.p13 chr17: 79,479,171-79,479,256 , GRCh38.p12 chr17: 81,512,145-81,512,230 FSCN2, ACTG1
    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
    nsv3913720copy number variation1nstd102humanPathogenic GRCh38 chr17: 81,008,196-83,102,584 , GRCh37 chr17: 78,981,996-81,048,189 , NCBI36 chr17: 76,596,591-78,653,749 LOC105376789, MIR4525, 89 more genes
    nsv3912269copy number variation1nstd102humanLikely pathogenic NCBI36 chr17: 76,990,361-78,635,227 , GRCh37 chr17: 79,375,766-81,041,938 , GRCh38 chr17: 81,401,966-83,084,062 ACTG1, ARHGDIA, 72 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 PRPSAP1, CACNG1, 1350 more genes
    nsv3911388copy number variation1nstd102humanPathogenic GRCh37 chr17: 76,914,732-80,978,971 , NCBI36 chr17: 74,426,327-78,572,260 , GRCh38 chr17: 78,918,650-83,021,095 ANAPC11, GPS1, 125 more genes
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