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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6871167copy number variation1nstd229human GRCh38 chr9: 119,925,406-119,940,012 , GRCh37.p13 chr9: 122,687,684-122,702,290 LINC01613, LOC107987122
    nsv6870537copy number variation1nstd229human GRCh38 chr9: 119,852,121-120,075,165 , GRCh37.p13 chr9: 122,614,399-122,837,443 LOC107987122, LOC107987123, 1 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6574762inversion1nstd223human GRCh38 chr9: 119,933,552-119,933,736 , GRCh37.p13 chr9: 122,695,830-122,696,014 LINC01613, LOC107987122
    nsv6446853copy number variation1nstd223human GRCh38 chr9: 119,926,163-119,935,498 , GRCh37.p13 chr9: 122,688,441-122,697,776 LOC107987122, LINC01613
    nsv6442034copy number variation1nstd223human GRCh38 chr9: 119,937,917-119,938,339 , GRCh37.p13 chr9: 122,700,195-122,700,617 LINC01613, LOC107987122
    nsv6314001copy number variation1nstd102humanPathogenic GRCh37 chr9: 116,422,275-131,713,233 , GRCh38.p12 chr9: 113,659,995-128,950,954 LOC105376244, RN7SL187P, 286 more genes
    nsv6313546copy number variation1nstd102humanPathogenic GRCh37 chr9: 353,349-141,020,389 , GRCh38.p12 chr9: 353,349-138,125,937 FAM27C, DPM2, 2166 more genes
    nsv6291398copy number variation1nstd102humanPathogenic GRCh37 chr9: 120,045,175-127,335,905 , GRCh38.p12 chr9: 117,282,896-124,573,626 ZBTB6, LOC105376253, 107 more genes
    nsv6290238copy number variation1nstd102humanUncertain significance GRCh37 chr9: 117,853,848-124,633,077 , GRCh38.p12 chr9: 115,091,569-121,870,798 LINC00474, LOC107987123, 72 more genes
    nsv6137050copy number variation1nstd213human GRCh37 chr9: 122,430,000-122,930,001 , GRCh38.p12 chr9: 119,667,722-120,167,723 LINC01613, LOC107987122, 1 more genes
    nsv5302636copy number variation1nstd204human GRCh37.p13 chr9: 122,614,394-122,837,449 , GRCh38.p13 chr9: 119,852,116-120,075,171 LINC01613, LOC107987122, 1 more genes
    nsv5253897copy number variation1nstd204human GRCh38.p13 chr9: 119,853,701-120,075,200 , GRCh37.p13 chr9: 122,615,979-122,837,478 LOC107987123, LINC01613, 1 more genes
    nsv5040732inversion1nstd200human GRCh38 chr9: 100,673,006-127,581,711 , GRCh37.p13 chr9: 103,435,288-130,343,990 , LOC105379839, 440 more genes
    nsv4983467copy number variation1nstd200human GRCh38 chr9: 119,852,120-120,075,164 , GRCh37.p13 chr9: 122,614,398-122,837,442 LOC107987122, LINC01613, 1 more genes
    nsv4836944copy number variation1nstd200human GRCh37 chr9: 122,614,399-122,837,442 , GRCh38.p12 chr9: 119,852,121-120,075,164 LOC107987123, LOC107987122, 1 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 more genes
    nsv4337085sequence alteration1nstd166human GRCh37.p13 chr9: 91,988,635-138,279,888 , GRCh38.p12 chr9: 89,373,720-135,388,042 , ABCA1, 927 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 TDRD7, CDK9, 2170 more genes
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