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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146530insertion1nstd232human GRCh37.p13 chr1: 95,690,522-95,690,522 , GRCh38.p12 chr1: 95,224,966-95,224,966 TLCD4-RWDD3, RWDD3-DT
    nsv7099217copy number variation1nstd231human GRCh38.p12 chr1: 95,215,497-95,402,283 , GRCh37 chr1: 95,681,053-95,867,839 RWDD3, TLCD4-RWDD3, 6 more genes
    nsv7099215copy number variation1nstd231human GRCh38.p12 chr1: 84,991,383-97,594,649 , GRCh37 chr1: 85,457,066-98,060,205 ABCA4, BRDT, 220 more genes
    nsv6657605copy number variation1nstd229human GRCh38 chr1: 95,233,998-95,239,856 , GRCh37.p13 chr1: 95,699,554-95,705,412 RWDD3, RWDD3-DT, 1 more genes
    nsv6657604copy number variation1nstd229human GRCh38 chr1: 95,224,968-95,225,273 , GRCh37.p13 chr1: 95,690,524-95,690,829 TLCD4-RWDD3, RWDD3-DT
    nsv6657602copy number variation1nstd229human GRCh38 chr1: 95,176,018-95,181,022 , GRCh37.p13 chr1: 95,641,574-95,646,578 RWDD3-DT, TLCD4-RWDD3, 1 more genes
    nsv6657601copy number variation1nstd229human GRCh38 chr1: 95,174,844-95,176,233 , GRCh37.p13 chr1: 95,640,400-95,641,789 TLCD4, TLCD4-RWDD3, 1 more genes
    nsv6657502copy number variation1nstd229human GRCh38 chr1: 95,212,683-95,212,714 , GRCh37.p13 chr1: 95,678,239-95,678,270 TLCD4-RWDD3, RWDD3-DT
    nsv6657501copy number variation1nstd229human GRCh38 chr1: 95,152,824-95,201,912 , GRCh37.p13 chr1: 95,618,380-95,667,468 TLCD4, RWDD3-DT, 1 more genes
    nsv6548823inversion1nstd223human GRCh38 chr1: 95,200,585-95,201,591 , GRCh37.p13 chr1: 95,666,141-95,667,147 TLCD4-RWDD3, RWDD3-DT
    nsv6334114copy number variation1nstd223human GRCh38 chr1: 95,203,781-95,204,186 , GRCh37.p13 chr1: 95,669,337-95,669,742 RWDD3-DT, TLCD4-RWDD3
    nsv6322887copy number variation1nstd223human GRCh38 chr1: 95,224,954-95,225,273 , GRCh37.p13 chr1: 95,690,510-95,690,829 RWDD3-DT, TLCD4-RWDD3
    nsv6321604copy number variation1nstd223human GRCh38 chr1: 95,170,363-95,170,695 , GRCh37.p13 chr1: 95,635,919-95,636,251 TLCD4-RWDD3, RWDD3-DT, 1 more genes
    nsv6317490copy number variation1nstd223human GRCh38 chr1: 95,197,809-95,198,230 , GRCh37.p13 chr1: 95,663,365-95,663,786 TLCD4-RWDD3, RWDD3-DT, 1 more genes
    nsv6316463copy number variation1nstd223human GRCh38 chr1: 95,193,501-95,195,100 , GRCh37.p13 chr1: 95,659,057-95,660,656 TLCD4, TLCD4-RWDD3, 1 more genes
    nsv6313675copy number variation1nstd102humanPathogenic GRCh37 chr1: 95,046,805-114,714,931 , GRCh38.p12 chr1: 94,581,249-114,172,309 LINC01307, FTLP17, 320 more genes
    nsv6147301sequence alteration1nstd206human GRCh38 chr1: 95,162,216-95,162,471 , GRCh37.p13 chr1: 95,627,772-95,628,027 TLCD4, TLCD4-RWDD3, 1 more genes
    nsv5985465copy number variation1nstd212human GRCh38 chr1: 95,218,516-95,219,780 , GRCh37.p13 chr1: 95,684,072-95,685,336 TLCD4-RWDD3, RWDD3-DT
    nsv5985133copy number variation1nstd212human GRCh38 chr1: 95,219,793-95,220,796 , GRCh37.p13 chr1: 95,685,349-95,686,352 TLCD4-RWDD3, RWDD3-DT
    nsv5985003copy number variation1nstd212human GRCh38 chr1: 95,224,954-95,225,273 , GRCh37.p13 chr1: 95,690,510-95,690,829 TLCD4-RWDD3, RWDD3-DT
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