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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7063062inversion1nstd229human GRCh38 chr9: 22,592,329-32,576,343 , GRCh37.p13 chr9: 22,592,328-32,576,341 HSPA8P17, RMRPP5, 81 more genes
    nsv7061226inversion1nstd229human GRCh38 chr9: 28,564,394-28,689,251 , GRCh37.p13 chr9: 28,564,392-28,689,249 KCTD10P1, LOC105376004, 2 more genes
    nsv6877907copy number variation1nstd229human GRCh38 chr9: 28,451,817-28,786,873 , GRCh37.p13 chr9: 28,451,815-28,786,871 LOC105376003, LINGO2, 2 more genes
    nsv6877527copy number variation1nstd229human GRCh38 chr9: 28,508,043-28,734,018 , GRCh37.p13 chr9: 28,508,041-28,734,016 LOC105376003, KCTD10P1, 2 more genes
    nsv6877236copy number variation1nstd229human GRCh38 chr9: 28,584,201-28,698,900 , GRCh37.p13 chr9: 28,584,199-28,698,898 LOC105376003, KCTD10P1, 2 more genes
    nsv6876637copy number variation1nstd229human GRCh38 chr9: 28,566,525-28,621,507 , GRCh37.p13 chr9: 28,566,523-28,621,505 LOC105376003, LOC105376004, 2 more genes
    nsv6876287copy number variation1nstd229human GRCh38 chr9: 28,593,932-28,800,929 , GRCh37.p13 chr9: 28,593,930-28,800,927 KCTD10P1, LINGO2, 2 more genes
    nsv6876235copy number variation1nstd229human GRCh38 chr9: 28,563,620-28,622,107 , GRCh37.p13 chr9: 28,563,618-28,622,105 LINGO2, KCTD10P1, 2 more genes
    nsv6875942copy number variation1nstd229human GRCh38 chr9: 24,741,564-30,889,392 , GRCh37.p13 chr9: 24,741,562-30,889,390 IFNK, LINC01242, 46 more genes
    nsv6875929copy number variation1nstd229human GRCh38 chr9: 28,513,701-28,742,900 , GRCh37.p13 chr9: 28,513,699-28,742,898 LINGO2, LOC105376003, 2 more genes
    nsv6875668copy number variation1nstd229human GRCh38 chr9: 28,537,184-28,605,685 , GRCh37.p13 chr9: 28,537,182-28,605,683 LINGO2, KCTD10P1, 1 more genes
    nsv6875437copy number variation1nstd229human GRCh38 chr9: 28,588,201-28,812,600 , GRCh37.p13 chr9: 28,588,199-28,812,598 KCTD10P1, LINGO2, 2 more genes
    nsv6874717copy number variation1nstd229human GRCh38 chr9: 28,596,052-28,597,688 , GRCh37.p13 chr9: 28,596,050-28,597,686 KCTD10P1, LOC105376004, 1 more genes
    nsv6874144copy number variation1nstd229human GRCh38 chr9: 28,521,001-28,722,200 , GRCh37.p13 chr9: 28,520,999-28,722,198 LOC105376003, LOC105376004, 2 more genes
    nsv6874057copy number variation1nstd229human GRCh38 chr9: 28,494,318-28,653,351 , GRCh37.p13 chr9: 28,494,316-28,653,349 LINGO2, KCTD10P1, 2 more genes
    nsv6873722copy number variation1nstd229human GRCh38 chr9: 28,572,269-28,642,340 , GRCh37.p13 chr9: 28,572,267-28,642,338 LOC105376003, LOC105376004, 2 more genes
    nsv6873383copy number variation1nstd229human GRCh38 chr9: 28,421,753-28,649,003 , GRCh37.p13 chr9: 28,421,751-28,649,001 LOC105376004, LINGO2, 2 more genes
    nsv6873354copy number variation1nstd229human GRCh38 chr9: 28,528,074-28,795,834 , GRCh37.p13 chr9: 28,528,072-28,795,832 LOC105376003, LOC105376004, 2 more genes
    nsv6872846copy number variation1nstd229human GRCh38 chr9: 28,564,459-28,643,809 , GRCh37.p13 chr9: 28,564,457-28,643,807 LOC105376003, KCTD10P1, 2 more genes
    nsv6872474copy number variation1nstd229human GRCh38 chr9: 28,516,654-28,800,254 , GRCh37.p13 chr9: 28,516,652-28,800,252 LINGO2, KCTD10P1, 2 more genes
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