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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130942insertion1nstd186human GRCh37 chr17: 14,216,462-14,216,475 , GRCh38.p12 chr17: 14,313,145-14,313,158 HS3ST3B1
    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
    nsv5976522insertion1nstd209human GRCh38 chr17: 14,313,108-14,313,108 , GRCh37.p13 chr17: 14,216,425-14,216,425 HS3ST3B1
    nsv5939662copy number variation1nstd209human GRCh38 chr17: 14,337,600-14,338,705 , GRCh37.p13 chr17: 14,240,917-14,242,022 HS3ST3B1
    nsv5882711copy number variation1nstd209human GRCh38 chr17: 14,337,568-14,338,767 , GRCh37.p13 chr17: 14,240,885-14,242,084 HS3ST3B1
    nsv5661906insertion1nstd207human GRCh38 chr17: 14,313,102-14,313,102 , GRCh37.p13 chr17: 14,216,419-14,216,419 HS3ST3B1
    nsv5595743copy number variation1nstd207human GRCh38 chr17: 14,337,600-14,338,705 , GRCh37.p13 chr17: 14,240,917-14,242,022 HS3ST3B1
    nsv5591158copy number variation1nstd207human GRCh38 chr17: 14,342,358-14,342,752 , GRCh37.p13 chr17: 14,245,675-14,246,069 HS3ST3B1
    nsv5534384insertion1nstd206human GRCh38 chr17: 14,313,145-14,313,158 , GRCh37.p13 chr17: 14,216,462-14,216,475 HS3ST3B1
    nsv5522380copy number variation1nstd206human GRCh38 chr17: 14,337,602-14,338,728 , GRCh37.p13 chr17: 14,240,919-14,242,045 HS3ST3B1
    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
    nsv5517315copy number variation1nstd206human GRCh38 chr17: 14,342,341-14,342,754 , GRCh37.p13 chr17: 14,245,658-14,246,071 HS3ST3B1
    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
    nsv5025968copy number variation1nstd200human GRCh38 chr17: 14,337,624-14,338,706 , GRCh37.p13 chr17: 14,240,941-14,242,023 HS3ST3B1
    nsv5025967copy number variation1nstd200human GRCh38 chr17: 14,319,612-14,319,689 , GRCh37.p13 chr17: 14,222,929-14,223,006 HS3ST3B1
    nsv5025966copy number variation1nstd200human GRCh38 chr17: 14,318,225-14,319,179 , GRCh37.p13 chr17: 14,221,542-14,222,496 HS3ST3B1
    nsv5025965copy number variation1nstd200human GRCh38 chr17: 14,308,049-14,314,465 , GRCh37.p13 chr17: 14,211,366-14,217,782 HS3ST3B1
    nsv5023694copy number variation1nstd200human GRCh38 chr17: 14,312,937-14,314,140 , GRCh37.p13 chr17: 14,216,254-14,217,457 HS3ST3B1
    nsv4858140copy number variation1nstd200human GRCh37 chr17: 14,240,941-14,242,023 , GRCh38.p12 chr17: 14,337,624-14,338,706 HS3ST3B1
    nsv4858139copy number variation1nstd200human GRCh37 chr17: 14,222,929-14,223,006 , GRCh38.p12 chr17: 14,319,612-14,319,689 HS3ST3B1
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