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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6114382mobile element insertion1nstd186human GRCh37 chr17: 58,048,616-58,048,667 , GRCh38.p12 chr17: 59,971,255-59,971,306 RNFT1-DT, TBC1D3P1-DHX40P1
    nsv5930800copy number variation1nstd209human GRCh38 chr17: 59,969,042-59,970,307 , GRCh37.p13 chr17: 58,046,403-58,047,668 TBC1D3P1-DHX40P1, RNFT1-DT
    nsv5928416copy number variation1nstd209human GRCh38 chr17: 59,984,794-60,002,833 , GRCh37.p13 chr17: 58,062,155-58,080,194 TBC1D3P1-DHX40P1, RNFT1-DT, 1 more genes
    nsv5883960copy number variation2nstd209human GRCh38 chr17: 59,983,272-59,991,551 , GRCh37.p13 chr17: 58,060,633-58,068,912 DHX40P1, RNFT1-DT, 1 more genes
    nsv5883650copy number variation2nstd209human GRCh38 chr17: 59,984,801-59,989,625 , GRCh37.p13 chr17: 58,062,162-58,066,986 TBC1D3P1-DHX40P1, DHX40P1, 1 more genes
    nsv5881950copy number variation2nstd209human GRCh38 chr17: 59,987,328-59,989,625 , GRCh37.p13 chr17: 58,064,689-58,066,986 RNFT1-DT, TBC1D3P1-DHX40P1, 1 more genes
    nsv5878652copy number variation1nstd209human GRCh38 chr17: 59,982,917-59,985,498 , GRCh37.p13 chr17: 58,060,278-58,062,859 DHX40P1, TBC1D3P1-DHX40P1, 1 more genes
    nsv5872860copy number variation1nstd209human GRCh38 chr17: 59,969,034-59,970,333 , GRCh37.p13 chr17: 58,046,395-58,047,694 TBC1D3P1-DHX40P1, RNFT1-DT
    nsv5711765mobile element insertion2nstd211human GRCh38 chr17: 59,971,255-59,971,255 , GRCh37.p13 chr17: 58,048,616-58,048,616 RNFT1-DT, TBC1D3P1-DHX40P1
    nsv5660749insertion1nstd207human GRCh38 chr17: 59,971,236-59,971,236 , GRCh37.p13 chr17: 58,048,597-58,048,597 RNFT1-DT, TBC1D3P1-DHX40P1
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5525706copy number variation1nstd206human GRCh38 chr17: 59,969,082-59,969,995 , GRCh37.p13 chr17: 58,046,443-58,047,356 RNFT1-DT, TBC1D3P1-DHX40P1
    nsv5524314copy number variation1nstd206human GRCh38 chr17: 59,984,754-60,003,049 , GRCh37.p13 chr17: 58,062,115-58,080,410 RNFT1-DT, DHX40P1, 1 more genes
    nsv5520634copy number variation1nstd206human GRCh38 chr17: 59,975,980-59,989,990 , GRCh37.p13 chr17: 58,053,341-58,067,351 TBC1D3P1-DHX40P1, RNFT1-DT, 1 more genes
    nsv5515453copy number variation1nstd206human GRCh38 chr17: 59,981,980-59,993,980 , GRCh37.p13 chr17: 58,059,341-58,071,341 DHX40P1, TBC1D3P1-DHX40P1, 1 more genes
    nsv5430731mobile element insertion1nstd206human GRCh38 chr17: 59,971,255-59,971,306 , GRCh37.p13 chr17: 58,048,616-58,048,667 TBC1D3P1-DHX40P1, RNFT1-DT
    nsv5374975translocation1nstd200human GRCh38 chr17: 59,971,617-59,971,617 , GRCh38 chr17: 59,963,907-59,963,907 , GRCh37.p13 chr17: 58,048,978-58,048,978 , GRCh37.p13 chr17: 58,041,268-58,041,268 RNFT1, TBC1D3P1-DHX40P1, 1 more genes
    nsv5300003copy number variation1nstd204human GRCh38.p13 chr17: 59,997,201-60,000,900 , GRCh37.p13 chr17: 58,074,562-58,078,261 DHX40P1, TBC1D3P1-DHX40P1, 1 more genes
    nsv5291483copy number variation1nstd204human GRCh38.p13 chr17: 59,982,901-60,001,100 , GRCh37.p13 chr17: 58,060,262-58,078,461 RNFT1-DT, DHX40P1, 1 more genes
    nsv5285898copy number variation1nstd204human GRCh38.p13 chr17: 59,983,543-59,986,298 , GRCh37.p13 chr17: 58,060,904-58,063,659 DHX40P1, RNFT1-DT, 1 more genes
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