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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950390insertion1nstd209human GRCh38 chr9: 98,119,801-98,119,801 , GRCh37.p13 chr9: 100,882,083-100,882,083 CORO2A, TRIM14
    nsv5697500mobile element insertion1nstd211human GRCh38 chr9: 98,079,549-98,079,549 , GRCh37.p13 chr9: 100,841,831-100,841,831 TRIM14, NANS
    nsv5489451copy number variation1nstd206human GRCh38 chr9: 98,071,724-98,109,618 , GRCh37.p13 chr9: 100,834,006-100,871,900 TRIM14, NANS
    nsv5485094copy number variation1nstd206human GRCh38 chr9: 98,084,146-98,087,105 , GRCh37.p13 chr9: 100,846,428-100,849,387 TRIM14
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 TBC1D2, ZNF782, 170 more genes
    nsv5378503translocation1nstd200human GRCh38 chr1: 107,921,728-107,921,728 , GRCh38 chr9: 98,084,363-98,084,363 , GRCh37.p13 chr9: 100,846,645-100,846,645 , GRCh37.p13 chr1: 108,464,350-108,464,350 TRIM14, VAV3
    nsv5330994translocation1nstd200human GRCh37 chr9: 100,846,645-100,846,645 , GRCh37 chr1: 108,464,350-108,464,350 , GRCh38.p12 chr1: 107,921,728-107,921,728 , GRCh38.p12 chr9: 98,084,363-98,084,363 TRIM14, VAV3
    nsv5250239copy number variation1nstd204human GRCh38.p13 chr9: 98,084,107-98,086,831 , GRCh37.p13 chr9: 100,846,389-100,849,113 TRIM14
    nsv5195971mobile element insertion1nstd203human GRCh38 chr9: 98,089,491-98,089,498 , GRCh37.p13 chr9: 100,851,773-100,851,780 TRIM14
    nsv5189558mobile element insertion1nstd203human GRCh38 chr9: 98,106,176-98,106,192 , GRCh37.p13 chr9: 100,868,458-100,868,474 TRIM14
    nsv5139541mobile element insertion1nstd203human GRCh38 chr9: 98,079,534-98,079,549 , GRCh37.p13 chr9: 100,841,816-100,841,831 TRIM14, NANS
    nsv5135045mobile element insertion1nstd203human GRCh38 chr9: 98,103,498-98,103,513 , GRCh37.p13 chr9: 100,865,780-100,865,795 TRIM14
    nsv5134515mobile element insertion1nstd203human GRCh38 chr9: 98,079,539-98,079,548 , GRCh37.p13 chr9: 100,841,821-100,841,830 TRIM14, NANS
    nsv5130729mobile element insertion1nstd203human GRCh38 chr9: 98,083,766-98,083,779 , GRCh37.p13 chr9: 100,846,048-100,846,061 TRIM14
    nsv5127076mobile element insertion1nstd203human GRCh38 chr9: 98,119,808-98,119,832 , GRCh37.p13 chr9: 100,882,090-100,882,114 CORO2A, TRIM14
    nsv5123727mobile element insertion1nstd203human GRCh38 chr9: 98,119,802-98,119,832 , GRCh37.p13 chr9: 100,882,084-100,882,114 TRIM14, CORO2A
    nsv4982714copy number variation1nstd200human GRCh38 chr9: 98,114,379-98,116,193 , GRCh37.p13 chr9: 100,876,661-100,878,475 TRIM14
    nsv4982713copy number variation1nstd200human GRCh38 chr9: 98,098,698-98,121,810 , GRCh37.p13 chr9: 100,860,980-100,884,092 TRIM14, CORO2A
    nsv4982712copy number variation1nstd200human GRCh38 chr9: 98,079,651-98,079,744 , GRCh37.p13 chr9: 100,841,933-100,842,026 NANS, TRIM14
    nsv4982711copy number variation1nstd200human GRCh38 chr9: 98,078,798-98,080,237 , GRCh37.p13 chr9: 100,841,080-100,842,519 NANS, TRIM14
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