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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5702331mobile element insertion2nstd211human GRCh38 chr17: 50,862,216-50,862,216 , GRCh37.p13 chr17: 48,939,577-48,939,577 TOB1
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5430229mobile element insertion1nstd206human GRCh38 chr17: 50,862,203-50,862,203 , GRCh37.p13 chr17: 48,939,564-48,939,564 TOB1
    nsv5322090copy number variation1nstd204human GRCh38.p13 chr17: 50,857,652-50,860,401 , GRCh37.p13 chr17: 48,935,013-48,937,762 TOB1
    nsv5289410copy number variation1nstd204human GRCh38.p13 chr17: 50,857,659-50,860,358 , GRCh37.p13 chr17: 48,935,020-48,937,719 TOB1
    nsv5156996mobile element insertion1nstd203human GRCh38 chr17: 50,862,208-50,862,216 , GRCh37.p13 chr17: 48,939,569-48,939,577 TOB1
    nsv5153327mobile element insertion1nstd203human GRCh38 chr17: 50,862,203-50,862,216 , GRCh37.p13 chr17: 48,939,564-48,939,577 TOB1
    nsv5140775mobile element insertion1nstd203human GRCh38 chr17: 50,862,202-50,862,216 , GRCh37.p13 chr17: 48,939,563-48,939,577 TOB1
    nsv5026399copy number variation1nstd200human GRCh38 chr17: 50,857,662-50,860,395 , GRCh37.p13 chr17: 48,935,023-48,937,756 TOB1
    nsv4867269copy number variation1nstd200human GRCh37 chr17: 48,935,022-48,937,757 , GRCh38.p12 chr17: 50,857,661-50,860,396 TOB1
    nsv4631608copy number variation1nstd183human GRCh37 chr17: 48,939,734-48,940,181 , GRCh38.p12 chr17: 50,862,373-50,862,820 TOB1
    nsv4508603mobile element insertion1nstd166human GRCh37.p13 chr17: 48,939,564-48,939,564 , GRCh38.p12 chr17: 50,862,203-50,862,203 TOB1
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4269957copy number variation1nstd166human GRCh37.p13 chr17: 48,930,000-48,954,000 , GRCh38.p12 chr17: 50,852,639-50,876,639 TOB1-AS1, TOB1
    nsv4259752copy number variation1nstd166human GRCh37.p13 chr17: 48,941,000-48,946,000 , GRCh38.p12 chr17: 50,863,639-50,868,639 TOB1-AS1, TOB1
    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
    nsv3912763copy number variation1nstd102humanPathogenic NCBI36 chr17: 44,570,225-47,580,169 , GRCh37 chr17: 47,215,226-50,225,170 , GRCh38 chr17: 49,137,864-52,147,810 CACNA1G, SUMO2P7, 77 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
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