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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7072464inversion1nstd229human GRCh38 chr17: 48,597,908-48,598,034 , GRCh37.p13 chr17: 46,675,270-46,675,396 HOXB6, HOXB-AS3
    nsv7065754inversion1nstd229human GRCh38 chr17: 48,536,987-48,650,780 , GRCh37.p13 chr17: 46,614,349-46,728,142 MIR196A1, HOXB4, 11 more genes
    nsv7058105inversion1nstd229human GRCh38 chr17: 48,590,046-48,595,764 , GRCh37.p13 chr17: 46,667,408-46,673,126 HOXB5, HOXB3, 2 more genes
    nsv6996133copy number variation1nstd229human GRCh38 chr17: 48,573,301-48,654,800 , GRCh37.p13 chr17: 46,650,663-46,732,162 LINC02086, MIR196A1, 10 more genes
    nsv6993659copy number variation1nstd229human GRCh38 chr17: 48,601,162-48,601,282 , GRCh37.p13 chr17: 46,678,524-46,678,644 HOXB6, HOXB-AS3
    nsv6988917copy number variation1nstd229human GRCh38 chr17: 48,595,804-48,595,914 , GRCh37.p13 chr17: 46,673,166-46,673,276 HOXB6, HOXB-AS3
    nsv6289076insertion1nstd214human GRCh37.p13 chr17: 46,666,847-46,666,847 , GRCh38 chr17: 48,589,485-48,589,485 HOXB3, HOXB5, 1 more genes
    nsv5928631copy number variation1nstd209human GRCh38 chr17: 48,601,162-48,601,281 , GRCh37.p13 chr17: 46,678,524-46,678,643 HOXB6, HOXB-AS3
    nsv5651369insertion1nstd207human GRCh38 chr17: 48,601,162-48,601,162 , GRCh37.p13 chr17: 46,678,524-46,678,524 HOXB6, HOXB-AS3
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5530046copy number variation1nstd206human GRCh38 chr17: 48,601,162-48,601,287 , GRCh37.p13 chr17: 46,678,524-46,678,649 HOXB6, HOXB-AS3
    nsv4864698copy number variation1nstd200human GRCh37 chr17: 46,678,524-46,678,649 , GRCh38.p12 chr17: 48,601,162-48,601,287 HOXB6, HOXB-AS3
    nsv4651375copy number variation3nstd186human GRCh37 chr17: 46,678,524-46,678,649 , GRCh38.p12 chr17: 48,601,162-48,601,287 HOXB-AS3, HOXB6
    nsv4555602insertion1nstd166human GRCh37.p13 chr17: 46,673,166-46,673,166 , GRCh38.p12 chr17: 48,595,804-48,595,804 HOXB6, HOXB-AS3
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4259796copy number variation1nstd166human GRCh37.p13 chr17: 46,678,524-46,678,649 , GRCh38.p12 chr17: 48,601,162-48,601,287 HOXB6, HOXB-AS3
    nsv3920056copy number variation1nstd102humanUncertain significance NCBI36 chr17: 43,882,989-44,985,282 , GRCh38 chr17: 48,450,628-49,552,921 , GRCh37 chr17: 46,527,990-47,630,283 ZNF652-AS1, RPS10P25, 55 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
    nsv3913486copy number variation1nstd102humanPathogenic GRCh38 chr17: 48,520,885-49,511,208 , NCBI36 chr17: 43,953,246-44,943,569 , GRCh37 chr17: 46,598,247-47,588,570 MIR6165, NGFR, 54 more genes
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