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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5867660copy number variation2nstd209human GRCh38 chr17: 35,410,122-35,412,521 , GRCh37.p13 chr17: 33,737,141-33,739,540 SLFN12
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5527387copy number variation1nstd206human GRCh38 chr17: 35,353,740-35,442,000 , GRCh37.p13 chr17: 33,680,759-33,769,019 SLFN12, SLFN11, 4 more genes
    nsv5515869copy number variation1nstd206human GRCh38 chr17: 35,353,800-35,441,980 , GRCh37.p13 chr17: 33,680,819-33,768,999 SLFN12, SLFN11, 4 more genes
    nsv5299389copy number variation1nstd204human GRCh38.p13 chr17: 35,422,491-35,423,590 , GRCh37.p13 chr17: 33,749,510-33,750,609 SLFN12
    nsv5295208copy number variation1nstd204human GRCh37.p13 chr17: 33,680,620-33,768,619 , GRCh38.p13 chr17: 35,353,601-35,441,600 SLFN12, SLFN11, 4 more genes
    nsv5292910copy number variation1nstd204human GRCh38.p13 chr17: 35,415,101-35,417,400 , GRCh37.p13 chr17: 33,742,120-33,744,419 SLFN12
    nsv5292221copy number variation1nstd204human GRCh38.p13 chr17: 35,420,242-35,422,390 , GRCh37.p13 chr17: 33,747,261-33,749,409 SLFN12
    nsv5291412copy number variation1nstd204human GRCh38.p13 chr17: 35,417,322-35,426,337 , GRCh37.p13 chr17: 33,744,341-33,753,356 SLFN12
    nsv5288417copy number variation1nstd204human GRCh38.p13 chr17: 35,352,846-35,411,421 , GRCh37.p13 chr17: 33,679,865-33,738,440 LOC729839, SLFN11, 3 more genes
    nsv5287069copy number variation1nstd204human GRCh37.p13 chr17: 33,679,620-33,769,319 , GRCh38.p13 chr17: 35,352,601-35,442,300 SLFN12, SLFN11, 4 more genes
    nsv5284937copy number variation1nstd204human GRCh38.p13 chr17: 35,428,701-35,442,000 , GRCh37.p13 chr17: 33,755,720-33,769,019 SLFN12, SLFN13
    nsv5282898copy number variation1nstd204human GRCh38.p13 chr17: 35,433,001-35,441,800 , GRCh37.p13 chr17: 33,760,020-33,768,819 SLFN12, SLFN13
    nsv5281092copy number variation1nstd204human GRCh38.p13 chr17: 35,392,778-35,428,187 , GRCh37.p13 chr17: 33,719,797-33,755,206 LOC729839, SLFN12
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4675860copy number variation1nstd102humanUncertain significance GRCh37 chr17: 33,073,917-33,863,479 , GRCh38.p12 chr17: 34,746,898-35,536,460 RPL37P22, LIG3, 26 more genes
    nsv4632412copy number variation1nstd183human GRCh37 chr17: 33,680,941-33,768,583 , GRCh38.p12 chr17: 35,353,922-35,441,564 SLFN12, SLFN11, 4 more genes
    nsv4631184copy number variation1nstd183human GRCh37 chr17: 33,682,510-33,768,199 , GRCh38.p12 chr17: 35,355,491-35,441,180 SLFN12, SLFN11, 4 more genes
    nsv4628688copy number variation1nstd183human GRCh37 chr17: 33,680,924-33,768,583 , GRCh38.p12 chr17: 35,353,905-35,441,564 SLFN12, SLFN11, 4 more genes
    nsv4532623copy number variation1nstd166human GRCh37.p13 chr17: 33,680,998-33,768,000 , GRCh38.p12 chr17: 35,353,979-35,440,981 SLFN12, SLFN11, 4 more genes
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