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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076231inversion1nstd229human GRCh38 chr17: 69,015,631-73,552,061 , GRCh37.p13 chr17: 67,011,772-71,548,200 KCNJ2-AS1, ROCR, 52 more genes
    nsv7063183inversion1nstd229human GRCh38 chr17: 68,931,960-70,066,756 , GRCh37.p13 chr17: 66,928,101-68,062,897 LOC105371878, ABCA8, 18 more genes
    nsv6989696copy number variation1nstd229human GRCh38 chr17: 69,999,701-70,080,400 , GRCh37.p13 chr17: 67,995,842-68,076,541 KCNJ16, LOC105371881, 2 more genes
    nsv6638043copy number variation1nstd102humanUncertain significance GRCh37 chr17: 67,730,594-68,272,354 , GRCh38.p12 chr17: 69,734,453-70,276,213 LINC01483, KCNJ2, 8 more genes
    nsv6515883copy number variation1nstd223human GRCh38 chr17: 70,054,479-70,054,916 , GRCh37.p13 chr17: 68,050,620-68,051,057 LINC01028, LOC105371881
    nsv6515600copy number variation1nstd223human GRCh38 chr17: 70,056,382-70,057,061 , GRCh37.p13 chr17: 68,052,523-68,053,202 LINC01028, LOC105371881
    nsv6133070copy number variation1nstd213human GRCh37 chr17: 62,460,000-73,800,001 , GRCh38.p12 chr17: 64,464,645-75,803,920 APOH, CACNG1, 225 more genes
    nsv6098469insertion1nstd212human GRCh38 chr17: 70,063,865-70,063,865 , GRCh37.p13 chr17: 68,060,006-68,060,006 LOC105371881, LINC01028
    nsv6091103insertion1nstd212human GRCh38 chr17: 70,063,575-70,063,575 , GRCh37.p13 chr17: 68,059,716-68,059,716 LINC01028, LOC105371881
    nsv6089962insertion1nstd212human GRCh38 chr17: 70,063,861-70,063,861 , GRCh37.p13 chr17: 68,060,002-68,060,002 LOC105371881, LINC01028
    nsv6082928insertion1nstd212human GRCh38 chr17: 70,065,601-70,065,601 , GRCh37.p13 chr17: 68,061,742-68,061,742 LINC01028, LOC105371881
    nsv5979991insertion1nstd209human GRCh38 chr17: 70,063,891-70,063,891 , GRCh37.p13 chr17: 68,060,032-68,060,032 LOC105371881, LINC01028
    nsv5969787insertion1nstd209human GRCh38 chr17: 70,065,601-70,065,601 , GRCh37.p13 chr17: 68,061,742-68,061,742 LINC01028, LOC105371881
    nsv5708677mobile element insertion2nstd211human GRCh38 chr17: 70,061,603-70,061,603 , GRCh37.p13 chr17: 68,057,744-68,057,744 LOC105371881, LINC01028
    nsv5697341mobile element insertion1nstd211human GRCh38 chr17: 70,058,795-70,058,795 , GRCh37.p13 chr17: 68,054,936-68,054,936 LINC01028, LOC105371881
    nsv5661955insertion2nstd207human GRCh38 chr17: 70,063,865-70,063,865 , GRCh37.p13 chr17: 68,060,006-68,060,006 LINC01028, LOC105371881
    nsv5645529insertion1nstd207human GRCh38 chr17: 70,063,591-70,063,591 , GRCh37.p13 chr17: 68,059,732-68,059,732 LINC01028, LOC105371881
    nsv5562348sequence alteration1nstd206human GRCh38 chr17: 70,066,572-70,066,734 , GRCh37.p13 chr17: 68,062,713-68,062,875 LINC01028, LOC105371881
    nsv5537159insertion1nstd206human GRCh38 chr17: 70,065,601-70,065,601 , GRCh37.p13 chr17: 68,061,742-68,061,742 LINC01028, LOC105371881
    nsv5429312mobile element insertion1nstd206human GRCh38 chr17: 70,061,603-70,061,654 , GRCh37.p13 chr17: 68,057,744-68,057,795 LINC01028, LOC105371881
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