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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5910698copy number variation1nstd209human GRCh38 chr8: 103,119,633-103,119,724 , GRCh37.p13 chr8: 104,131,861-104,131,952 LINC01181
    nsv5718939mobile element insertion2nstd211human GRCh38 chr8: 103,134,559-103,134,559 , GRCh37.p13 chr8: 104,146,787-104,146,787 BAALC-AS2, LINC01181
    nsv5566845copy number variation1nstd207human GRCh38 chr8: 103,119,633-103,119,724 , GRCh37.p13 chr8: 104,131,861-104,131,952 LINC01181
    nsv5558580mobile element insertion1nstd206human GRCh38 chr8: 103,134,559-103,134,610 , GRCh37.p13 chr8: 104,146,787-104,146,838 BAALC-AS2, LINC01181
    nsv5484516copy number variation1nstd206human GRCh38 chr8: 103,119,910-103,123,426 , GRCh37.p13 chr8: 104,132,138-104,135,654 LINC01181
    nsv5481186copy number variation1nstd206human GRCh38 chr8: 103,119,636-103,119,725 , GRCh37.p13 chr8: 104,131,864-104,131,953 LINC01181
    nsv5372081translocation1nstd200human GRCh38 chr8: 103,119,910-103,119,910 , GRCh38 chr8: 103,123,426-103,123,426 , GRCh37.p13 chr8: 104,135,654-104,135,654 , GRCh37.p13 chr8: 104,132,138-104,132,138 LINC01181
    nsv5343516translocation1nstd200human GRCh37 chr8: 104,131,953-104,131,953 , GRCh37 chr8: 104,131,864-104,131,864 , GRCh38.p12 chr8: 103,119,636-103,119,636 , GRCh38.p12 chr8: 103,119,725-103,119,725 LINC01181
    nsv5039005inversion1nstd200human GRCh38 chr8: 102,793,534-107,480,712 , GRCh37.p13 chr8: 103,805,762-108,492,940 , LOC105375693, 58 more genes
    nsv5036483inversion1nstd200human GRCh38 chr8: 71,454,844-121,935,245 , GRCh37.p13 chr8: 72,367,079-122,947,484 , LINC01617, 636 more genes
    nsv5035989inversion1nstd200human GRCh38 chr8: 74,949,087-131,777,713 , GRCh37.p13 chr8: 75,861,322-132,789,960 , MIR7705, 715 more genes
    nsv4961617copy number variation1nstd200human GRCh38 chr8: 103,136,836-103,138,585 , GRCh37.p13 chr8: 104,149,064-104,150,813 LINC01181, BAALC-AS2
    nsv4874421inversion1nstd200human GRCh37 chr8: 103,805,762-108,492,940 , GRCh38.p12 chr8: 102,793,534-107,480,712 , ZFPM2, 58 more genes
    nsv4822707copy number variation1nstd200human GRCh37 chr8: 104,149,064-104,150,813 , GRCh38.p12 chr8: 103,136,836-103,138,585 BAALC-AS2, LINC01181
    nsv4822706copy number variation1nstd200human GRCh37 chr8: 104,132,138-104,135,654 , GRCh38.p12 chr8: 103,119,910-103,123,426 LINC01181
    nsv4617180copy number variation1nstd183human GRCh37 chr8: 104,110,835-105,017,954 , GRCh38.p12 chr8: 103,098,607-104,005,726 LOC105375689, RPS6P9, 17 more genes
    nsv4603412copy number variation1nstd183human GRCh37 chr8: 104,132,138-104,135,654 , GRCh38.p12 chr8: 103,119,910-103,123,426 LINC01181
    nsv4572692sequence alteration1nstd166human GRCh37.p13 chr8: 104,115,243-105,852,952 , GRCh38.p12 chr8: 103,103,015-104,840,724 SLC25A32, MIR548A3, 28 more genes
    nsv4526830copy number variation1nstd166human GRCh37.p13 chr8: 104,136,267-104,136,372 , GRCh38.p12 chr8: 103,124,039-103,124,144 LINC01181
    nsv4479200mobile element insertion1nstd166human GRCh37.p13 chr8: 104,152,487-104,152,487 , GRCh38.p12 chr8: 103,140,259-103,140,259 BAALC, BAALC-AS2, 1 more genes
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