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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5938611copy number variation1nstd209human GRCh38 chr17: 50,766,754-50,767,128 , GRCh37.p13 chr17: 48,844,115-48,844,489 ANKRD40CL, MIR8059
    nsv5594477copy number variation1nstd207human GRCh38 chr17: 50,766,754-50,767,128 , GRCh37.p13 chr17: 48,844,115-48,844,489 ANKRD40CL, MIR8059
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5526966copy number variation1nstd206human GRCh38 chr17: 50,766,757-50,767,129 , GRCh37.p13 chr17: 48,844,118-48,844,490 ANKRD40CL, MIR8059
    nsv5393318copy number variation3nstd186human GRCh37 chr17: 48,844,118-48,844,490 , GRCh38.p12 chr17: 50,766,757-50,767,129 ANKRD40CL, MIR8059
    nsv5320922copy number variation1nstd204human GRCh37.p13 chr17: 48,844,115-48,844,492 , GRCh38.p13 chr17: 50,766,754-50,767,131 ANKRD40CL, MIR8059
    nsv5026393copy number variation1nstd200human GRCh38 chr17: 50,766,757-50,767,129 , GRCh37.p13 chr17: 48,844,118-48,844,490 MIR8059, ANKRD40CL
    nsv4867263copy number variation1nstd200human GRCh37 chr17: 48,844,118-48,844,490 , GRCh38.p12 chr17: 50,766,757-50,767,129 MIR8059, ANKRD40CL
    nsv4706690copy number variation1nstd195human GRCh37 chr17: 48,844,115-48,844,116 , GRCh38.p12 chr17: 50,766,754-50,766,755 ANKRD40CL, MIR8059
    nsv4670094copy number variation1nstd186human GRCh37 chr17: 48,844,115-48,844,490 , GRCh38.p12 chr17: 50,766,754-50,767,129 ANKRD40CL, MIR8059
    nsv4641482copy number variation1nstd186human GRCh37 chr17: 48,844,118-48,844,503 , GRCh38.p12 chr17: 50,766,757-50,767,142 MIR8059, ANKRD40CL
    nsv4635382copy number variation1nstd186human GRCh37 chr17: 48,844,118-48,844,533 , GRCh38.p12 chr17: 50,766,757-50,767,172 ANKRD40CL, MIR8059
    nsv4621211copy number variation1nstd183human GRCh37 chr17: 48,844,115-48,844,490 , GRCh38.p12 chr17: 50,766,754-50,767,129 ANKRD40CL, MIR8059
    nsv4531567copy number variation1nstd166human GRCh37.p13 chr17: 48,844,118-48,844,533 , GRCh38.p12 chr17: 50,766,757-50,767,172 ANKRD40CL, MIR8059
    nsv4414615copy number variation1nstd174human GRCh37 chr17: 48,844,115-48,844,503 , GRCh38.p12 chr17: 50,766,754-50,767,142 MIR8059, ANKRD40CL
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4271774copy number variation1nstd166human GRCh37.p13 chr17: 48,821,000-48,847,000 , GRCh38.p12 chr17: 50,743,639-50,769,639 ANKRD40CL, MIR8059, 1 more genes
    nsv3920880copy number variation1nstd102humanPathogenic GRCh38 chr17: 49,974,533-56,807,609 , NCBI36 chr17: 45,406,896-52,239,969 , GRCh37 chr17: 48,051,897-54,884,970 LOC107984983, LOC102724732, 85 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
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 more genes
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