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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112783copy number variation1nstd102humannot provided GRCh37 chr17: 15,133,096-15,164,093 , GRCh38.p12 chr17: 15,229,779-15,260,776 PMP22, MIR4731
    nsv6112771copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,098,196-15,442,500 , GRCh38.p12 chr17: 14,194,879-15,539,186 CDRT8, TVP23C, 24 more genes
    nsv5980398copy number variation2nstd102humanPathogenic GRCh37 chr17: 15,134,233-15,164,044 , GRCh38.p12 chr17: 15,230,916-15,260,727 PMP22, MIR4731
    nsv5694509mobile element insertion1nstd211human GRCh38 chr17: 15,237,237-15,237,237 , GRCh37.p13 chr17: 15,140,554-15,140,554 PMP22
    nsv5673029copy number variation2nstd102humanPathogenic GRCh37 chr17: 15,134,234-15,164,044 , GRCh38.p12 chr17: 15,230,917-15,260,727 PMP22, MIR4731
    nsv5673028copy number variation2nstd102humanPathogenic GRCh37 chr17: 15,133,097-15,164,054 , GRCh38.p12 chr17: 15,229,780-15,260,737 PMP22, MIR4731
    nsv5673027copy number variation1nstd102humanPathogenic GRCh37 chr17: 15,132,094-15,169,674 , GRCh38.p12 chr17: 15,228,777-15,266,357 PMP22, MIR4731
    nsv5672958copy number variation2nstd102humanPathogenic GRCh37 chr17: 15,134,214-15,164,064 , GRCh38.p12 chr17: 15,230,897-15,260,747 PMP22, MIR4731
    nsv5672867copy number variation1nstd102humanPathogenic GRCh37 chr17: 15,162,401-15,162,520 , GRCh38.p12 chr17: 15,259,084-15,259,203 PMP22
    nsv5520330copy number variation1nstd206human GRCh38 chr17: 14,022,600-15,889,111 , GRCh37.p13 chr17: 13,925,917-15,792,425 CDRT15, CDRT7, 42 more genes
    nsv5426820mobile element insertion1nstd206human GRCh38 chr17: 15,237,237-15,237,288 , GRCh37.p13 chr17: 15,140,554-15,140,605 PMP22
    nsv5381804copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,100,118-15,455,297 , GRCh38.p12 chr17: 14,196,801-15,551,983 LOC105371547, TVP23C-CDRT4, 24 more genes
    nsv5315964copy number variation1nstd204human GRCh38.p13 chr17: 15,248,295-15,248,607 , GRCh37.p13 chr17: 15,151,612-15,151,924 PMP22
    nsv5026007copy number variation1nstd200human GRCh38 chr17: 15,262,971-15,277,715 , GRCh37.p13 chr17: 15,166,288-15,181,032 PMP22
    nsv4864537copy number variation1nstd200human GRCh37 chr17: 15,151,620-15,151,916 , GRCh38.p12 chr17: 15,248,303-15,248,599 PMP22
    nsv4858166copy number variation1nstd200human GRCh37 chr17: 15,166,288-15,181,032 , GRCh38.p12 chr17: 15,262,971-15,277,715 PMP22
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729887copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr17: 14,111,754-15,442,178 , GRCh38.p12 chr17: 14,208,437-15,538,864 CDRT15, LINC02096, 24 more genes
    nsv4684248copy number variation1nstd102humanPathogenic GRCh37 chr17: 14,079,630-15,370,444 , GRCh38.p12 chr17: 14,176,313-15,467,130 MIR4731, LOC107984996, 21 more genes
    nsv4683509copy number variation1nstd102humanPathogenic GRCh37 chr17: 15,133,084-15,142,938 , GRCh38.p12 chr17: 15,229,767-15,239,621 PMP22
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