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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095353copy number variation1nstd102humanUncertain significance GRCh37 chr17: 62,006,586-62,050,201 , GRCh38.p12 chr17: 63,929,226-63,972,841 CD79B, LOC105371858, 1 more genes
    nsv7077395inversion1nstd229human GRCh38 chr17: 63,953,218-63,978,383 , GRCh37.p13 chr17: 62,030,578-62,055,743 LOC105371858, SCN4A
    nsv7060106inversion1nstd229human GRCh38 chr17: 63,466,957-64,030,780 , GRCh37.p13 chr17: 61,544,318-62,108,140 LOC101927898, KCNH6, 30 more genes
    nsv6996338copy number variation1nstd229human GRCh38 chr17: 63,957,876-63,986,850 , GRCh37.p13 chr17: 62,035,236-62,064,210 SCN4A, LOC105371858
    nsv6986015copy number variation1nstd229human GRCh38 chr17: 63,901,401-64,077,400 , GRCh37.p13 chr17: 61,978,761-62,154,760 ERN1, PRR29-AS1, 8 more genes
    nsv6982752copy number variation1nstd229human GRCh38 chr17: 63,973,185-63,973,253 , GRCh37.p13 chr17: 62,050,545-62,050,613 SCN4A
    nsv6637179copy number variation1nstd102humanUncertain significance GRCh37 chr17: 61,838,634-62,465,444 , GRCh38.p12 chr17: 63,761,274-64,469,327 GH2, DDX42, 24 more genes
    nsv6528316copy number variation1nstd223human GRCh38 chr17: 63,969,765-63,970,686 , GRCh37.p13 chr17: 62,047,125-62,048,046 SCN4A
    nsv6527951copy number variation1nstd223human GRCh38 chr17: 63,957,876-63,986,846 , GRCh37.p13 chr17: 62,035,236-62,064,206 SCN4A, LOC105371858
    nsv6310328copy number variation1nstd102humanUncertain significance GRCh37 chr17: 62,048,502-62,050,201 , GRCh38.p12 chr17: 63,971,142-63,972,841 SCN4A
    nsv6310231copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,024,385-62,034,898 , GRCh38.p12 chr17: 63,947,025-63,957,538 SCN4A, LOC105371858
    nsv6133316copy number variation1nstd213human GRCh37 chr17: 53,930,000-62,410,001 , GRCh38.p12 chr17: 55,852,639-64,332,641 CA4, CD79B, 208 more genes
    nsv5980437copy number variation1nstd102humanLikely benign GRCh38 chr17: 63,963,578-63,963,662 , GRCh37 chr17: 62,040,938-62,041,022 LOC105371858, SCN4A
    nsv5929219copy number variation1nstd209human GRCh38 chr17: 63,956,317-63,956,367 , GRCh37.p13 chr17: 62,033,677-62,033,727 SCN4A
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5533377copy number variation1nstd206human GRCh38 chr17: 63,906,475-64,023,565 , GRCh37.p13 chr17: 61,983,835-62,100,925 CD79B, CSHL1, 7 more genes
    nsv5528400copy number variation1nstd206human GRCh38 chr17: 63,963,567-63,963,681 , GRCh37.p13 chr17: 62,040,927-62,041,041 LOC105371858, SCN4A
    nsv5516399copy number variation1nstd206human GRCh38 chr17: 63,969,752-63,970,729 , GRCh37.p13 chr17: 62,047,112-62,048,089 SCN4A
    nsv5321177copy number variation1nstd204human GRCh37.p13 chr17: 62,038,783-62,041,636 , GRCh38.p13 chr17: 63,961,423-63,964,276 LOC105371858, SCN4A
    nsv5294558copy number variation1nstd204human GRCh38.p13 chr17: 63,961,361-63,962,360 , GRCh37.p13 chr17: 62,038,721-62,039,720 LOC105371858, SCN4A
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