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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7058619inversion1nstd229human GRCh38 chr17: 49,389,100-51,159,770 , GRCh37.p13 chr17: 47,466,462-49,237,131 H1-9P, FLJ45513, 59 more genes
    nsv6986384copy number variation1nstd229human GRCh38 chr17: 49,089,556-55,863,152 , GRCh37.p13 chr17: 47,166,918-53,940,513 LOC107985002, FAM117A, 107 more genes
    nsv6519084copy number variation1nstd223human GRCh38 chr17: 50,350,142-50,350,526 , GRCh37.p13 chr17: 48,427,503-48,427,887 XYLT2
    nsv6305849copy number variation1nstd186human GRCh37 chr17: 48,427,538-48,427,883 , GRCh38.p12 chr17: 50,350,177-50,350,522 XYLT2
    nsv6144902copy number variation1nstd206human GRCh38 chr17: 50,350,157-50,350,546 , GRCh37.p13 chr17: 48,427,518-48,427,907 XYLT2
    nsv6032488copy number variation1nstd212human GRCh38 chr17: 50,350,142-50,350,534 , GRCh37.p13 chr17: 48,427,503-48,427,895 XYLT2
    nsv5929966copy number variation1nstd209human GRCh38 chr17: 50,350,142-50,350,525 , GRCh37.p13 chr17: 48,427,503-48,427,886 XYLT2
    nsv5729418mobile element insertion1nstd211human GRCh38 chr17: 50,359,721-50,359,721 , GRCh37.p13 chr17: 48,437,082-48,437,082 XYLT2
    nsv5586375copy number variation1nstd207human GRCh38 chr17: 50,350,142-50,350,525 , GRCh37.p13 chr17: 48,427,503-48,427,886 XYLT2
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5389681copy number variation1nstd186human GRCh37 chr17: 48,427,441-48,427,665 , GRCh38.p12 chr17: 50,350,080-50,350,304 XYLT2
    nsv5328311copy number variation1nstd204human GRCh38.p13 chr17: 50,350,281-50,350,560 , GRCh37.p13 chr17: 48,427,642-48,427,921 XYLT2
    nsv5282765copy number variation1nstd204human GRCh38.p13 chr17: 50,350,201-50,350,500 , GRCh37.p13 chr17: 48,427,562-48,427,861 XYLT2
    nsv5144793mobile element insertion1nstd203human GRCh38 chr17: 50,350,411-50,350,421 , GRCh37.p13 chr17: 48,427,772-48,427,782 XYLT2
    nsv5026382copy number variation1nstd200human GRCh38 chr17: 50,350,177-50,350,526 , GRCh37.p13 chr17: 48,427,538-48,427,887 XYLT2
    nsv4867255copy number variation1nstd200human GRCh37 chr17: 48,427,440-48,427,665 , GRCh38.p12 chr17: 50,350,079-50,350,304 XYLT2
    nsv4749677copy number variation1nstd199human GRCh37 chr17: 48,427,506-48,427,890 , GRCh38.p12 chr17: 50,350,145-50,350,529 XYLT2
    nsv4709605copy number variation2nstd195human GRCh37 chr17: 48,427,503-48,427,504 , GRCh38.p12 chr17: 50,350,142-50,350,143 XYLT2
    nsv4652254copy number variation2nstd186human GRCh37 chr17: 48,427,538-48,427,887 , GRCh38.p12 chr17: 50,350,177-50,350,526 XYLT2
    nsv4626640copy number variation1nstd183human GRCh37 chr17: 48,423,466-48,423,586 , GRCh38.p12 chr17: 50,346,105-50,346,225 XYLT2
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