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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098452copy number variation1nstd102humanUncertain significance GRCh37 chr9: 27,047,252-27,573,526 , GRCh38.p12 chr9: 27,047,254-27,573,528 LINC00032, RPL36AP34, 7 more genes
    nsv7067290inversion1nstd229human GRCh38 chr9: 27,371,556-27,371,650 , GRCh37.p13 chr9: 27,371,554-27,371,648 MOB3B
    nsv7063062inversion1nstd229human GRCh38 chr9: 22,592,329-32,576,343 , GRCh37.p13 chr9: 22,592,328-32,576,341 HSPA8P17, RMRPP5, 81 more genes
    nsv7061639inversion1nstd229human GRCh38 chr9: 27,464,374-27,476,026 , GRCh37.p13 chr9: 27,464,372-27,476,024 MOB3B
    nsv6877091copy number variation1nstd229human GRCh38 chr9: 27,306,697-27,372,966 , GRCh37.p13 chr9: 27,306,695-27,372,964 MOB3B
    nsv6877017copy number variation1nstd229human GRCh38 chr9: 27,416,686-27,422,465 , GRCh37.p13 chr9: 27,416,684-27,422,463 MOB3B
    nsv6876479copy number variation1nstd229human GRCh38 chr9: 27,415,503-27,415,703 , GRCh37.p13 chr9: 27,415,501-27,415,701 MOB3B
    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
    nsv6875566copy number variation1nstd229human GRCh38 chr9: 27,499,801-27,503,900 , GRCh37.p13 chr9: 27,499,799-27,503,898 MOB3B
    nsv6875309copy number variation1nstd229human GRCh38 chr9: 27,470,007-27,532,968 , GRCh37.p13 chr9: 27,470,005-27,532,966 MOB3B, IFNK
    nsv6875078copy number variation1nstd229human GRCh38 chr9: 27,486,948-27,492,413 , GRCh37.p13 chr9: 27,486,946-27,492,411 MOB3B
    nsv6874177copy number variation1nstd229human GRCh38 chr9: 27,527,497-27,527,561 , GRCh37.p13 chr9: 27,527,495-27,527,559 MOB3B
    nsv6873934copy number variation1nstd229human GRCh38 chr9: 27,219,727-27,378,626 , GRCh37.p13 chr9: 27,219,725-27,378,624 LINC00032, EQTN, 2 more genes
    nsv6871276copy number variation1nstd229human GRCh38 chr9: 27,271,791-27,330,180 , GRCh37.p13 chr9: 27,271,789-27,330,178 MOB3B, EQTN, 1 more genes
    nsv6870871copy number variation1nstd229human GRCh38 chr9: 27,362,666-27,547,359 , GRCh37.p13 chr9: 27,362,664-27,547,357 C9orf72, IFNK, 1 more genes
    nsv6870560copy number variation1nstd229human GRCh38 chr9: 27,420,562-27,441,467 , GRCh37.p13 chr9: 27,420,560-27,441,465 MOB3B
    nsv6869210copy number variation1nstd229human GRCh38 chr9: 27,329,598-27,329,860 , GRCh37.p13 chr9: 27,329,596-27,329,858 MOB3B
    nsv6869148copy number variation1nstd229human GRCh38 chr9: 27,329,639-27,379,306 , GRCh37.p13 chr9: 27,329,637-27,379,304 MOB3B
    nsv6866315copy number variation1nstd229human GRCh38 chr9: 27,327,724-27,442,430 , GRCh37.p13 chr9: 27,327,722-27,442,428 MOB3B
    nsv6865795copy number variation1nstd229human GRCh38 chr9: 27,222,635-27,546,484 , GRCh37.p13 chr9: 27,222,633-27,546,482 C9orf72, LINC00032, 4 more genes
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