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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6876929copy number variation1nstd229human GRCh38 chr9: 102,629,844-102,749,742 , GRCh37.p13 chr9: 105,392,126-105,512,024 LINC00587
    nsv6876850copy number variation1nstd229human GRCh38 chr9: 102,623,204-102,626,729 , GRCh37.p13 chr9: 105,385,486-105,389,011 LINC00587
    nsv6876845copy number variation1nstd229human GRCh38 chr9: 102,565,801-102,578,500 , GRCh37.p13 chr9: 105,328,083-105,340,782 LINC00587
    nsv6876277copy number variation1nstd229human GRCh38 chr9: 102,651,144-102,656,236 , GRCh37.p13 chr9: 105,413,426-105,418,518 LINC00587
    nsv6875412copy number variation1nstd229human GRCh38 chr9: 102,533,870-102,543,940 , GRCh37.p13 chr9: 105,296,152-105,306,222 LINC00587
    nsv6875338copy number variation1nstd229human GRCh38 chr9: 102,526,968-103,052,403 , GRCh37.p13 chr9: 105,289,250-105,814,685 ZYG11AP1, LINC00587, 2 more genes
    nsv6874758copy number variation1nstd229human GRCh38 chr9: 102,624,223-102,627,803 , GRCh37.p13 chr9: 105,386,505-105,390,085 LINC00587
    nsv6874679copy number variation1nstd229human GRCh38 chr9: 102,633,858-102,728,200 , GRCh37.p13 chr9: 105,396,140-105,490,482 LINC00587
    nsv6874187copy number variation1nstd229human GRCh38 chr9: 102,481,945-102,572,477 , GRCh37.p13 chr9: 105,244,227-105,334,759 LINC00587, LOC105376190, 1 more genes
    nsv6874012copy number variation1nstd229human GRCh38 chr9: 102,586,575-102,600,816 , GRCh37.p13 chr9: 105,348,857-105,363,098 LINC00587
    nsv6873949copy number variation1nstd229human GRCh38 chr9: 102,568,594-102,588,510 , GRCh37.p13 chr9: 105,330,876-105,350,792 LINC00587
    nsv6872974copy number variation1nstd229human GRCh38 chr9: 102,481,339-102,534,431 , GRCh37.p13 chr9: 105,243,621-105,296,713 LOC105376190, LINC00587, 1 more genes
    nsv6872208copy number variation1nstd229human GRCh38 chr9: 102,606,210-102,611,145 , GRCh37.p13 chr9: 105,368,492-105,373,427 LINC00587, ZYG11AP1
    nsv6871908copy number variation1nstd229human GRCh38 chr9: 102,205,593-103,465,031 , GRCh37.p13 chr9: 104,967,875-106,227,313 ZYG11AP1, LOC105376190, 8 more genes
    nsv6871756copy number variation1nstd229human GRCh38 chr9: 102,563,204-102,877,549 , GRCh37.p13 chr9: 105,325,486-105,639,831 ZYG11AP1, LINC00587
    nsv6871722copy number variation1nstd229human GRCh38 chr9: 102,615,901-102,619,200 , GRCh37.p13 chr9: 105,378,183-105,381,482 LINC00587
    nsv6871368copy number variation1nstd229human GRCh38 chr9: 102,548,337-102,607,262 , GRCh37.p13 chr9: 105,310,619-105,369,544 LINC00587
    nsv6870935copy number variation1nstd229human GRCh38 chr9: 102,568,267-102,594,807 , GRCh37.p13 chr9: 105,330,549-105,357,089 LINC00587
    nsv6870057copy number variation1nstd229human GRCh38 chr9: 102,608,601-103,050,800 , GRCh37.p13 chr9: 105,370,883-105,813,082 LOC100421294, CYLC2, 2 more genes
    nsv6868461copy number variation1nstd229human GRCh38 chr9: 102,537,986-102,547,875 , GRCh37.p13 chr9: 105,300,268-105,310,157 LINC00587
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