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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6117154mobile element insertion1nstd186human GRCh37 chr8: 11,225,300-11,225,300 , GRCh38.p12 chr8: 11,367,791-11,367,791 , GRCh38.p12 chr8|NW_018654717.1: 1,979,060-1,979,060 FAM167A-AS1, TDH
    nsv5922669copy number variation1nstd209human GRCh38 chr8: 11,437,698-11,437,813 , GRCh37.p13 chr8: 11,295,207-11,295,322 FAM167A-AS1, FAM167A
    nsv5918356copy number variation1nstd209human GRCh38 chr8: 11,370,850-11,371,762 , GRCh37.p13 chr8: 11,228,359-11,229,271 FAM167A-AS1
    nsv5917000copy number variation1nstd209human GRCh38 chr8: 11,377,436-11,451,484 , GRCh37.p13 chr8: 11,234,945-11,308,993 FAM167A, FAM167A-AS1, 2 more genes
    nsv5909380copy number variation1nstd209human GRCh38 chr8: 11,388,049-11,389,697 , GRCh37.p13 chr8: 11,245,558-11,247,206 FAM167A-AS1
    nsv5866037copy number variation2nstd209human GRCh38 chr8: 11,400,726-11,402,267 , GRCh37.p13 chr8: 11,258,235-11,259,776 FAM167A-AS1
    nsv5858480copy number variation2nstd209human GRCh38 chr8: 11,394,073-11,396,372 , GRCh37.p13 chr8: 11,251,582-11,253,881 FAM167A-AS1
    nsv5858476copy number variation1nstd209human GRCh38 chr8: 11,389,651-11,416,581 , GRCh37.p13 chr8: 11,247,160-11,274,090 RNU6-1084P, FAM167A-AS1
    nsv5855402copy number variation1nstd209human GRCh38 chr8: 11,377,538-11,388,125 , GRCh37.p13 chr8: 11,235,047-11,245,634 FAM167A-AS1, RN7SL293P
    nsv5855199copy number variation2nstd209human GRCh38 chr8: 11,382,026-11,383,025 , GRCh37.p13 chr8: 11,239,535-11,240,534 FAM167A-AS1
    nsv5853918copy number variation1nstd209human GRCh38 chr8: 11,388,026-11,389,725 , GRCh37.p13 chr8: 11,245,535-11,247,234 FAM167A-AS1
    nsv5696358mobile element insertion2nstd211human GRCh38 chr8: 11,367,807-11,367,807 , GRCh37.p13 chr8: 11,225,316-11,225,316 FAM167A-AS1, TDH
    nsv5671625inversion1nstd207human GRCh38 chr8: 7,301,025-12,600,730 , GRCh37.p13 chr8: 7,158,547-12,458,239 , BLK, 188 more genes
    nsv5626685insertion1nstd207human GRCh38 chr8: 11,437,698-11,437,698 , GRCh37.p13 chr8: 11,295,207-11,295,207 FAM167A, FAM167A-AS1
    nsv5625912insertion1nstd207human GRCh38 chr8: 11,367,791-11,367,791 , GRCh37.p13 chr8: 11,225,300-11,225,300 TDH, FAM167A-AS1
    nsv5579432copy number variation1nstd207human GRCh38 chr8: 11,406,460-11,406,513 , GRCh37.p13 chr8: 11,263,969-11,264,022 FAM167A-AS1
    nsv5566591copy number variation1nstd207human GRCh38 chr8: 11,388,049-11,389,697 , GRCh37.p13 chr8: 11,245,558-11,247,206 FAM167A-AS1
    nsv5490721copy number variation1nstd206human GRCh38 chr8: 11,373,916-11,373,967 , GRCh37.p13 chr8: 11,231,425-11,231,476 FAM167A-AS1
    nsv5489836copy number variation1nstd206human GRCh38 chr8: 11,388,052-11,389,698 , GRCh37.p13 chr8: 11,245,561-11,247,207 FAM167A-AS1
    nsv5485114copy number variation1nstd206human GRCh38 chr8: 11,390,996-11,391,071 , GRCh37.p13 chr8: 11,248,505-11,248,580 RNU6-1084P, FAM167A-AS1
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