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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5917634copy number variation1nstd209human GRCh38 chr9: 133,514,088-133,514,429 , GRCh37.p13 chr9: 136,379,210-136,379,551 MYMK
    nsv5595395copy number variation1nstd207human GRCh38 chr9: 133,514,088-133,514,429 , GRCh37.p13 chr9: 136,379,210-136,379,551 MYMK
    nsv5489828copy number variation1nstd206human GRCh38 chr9: 133,514,100-133,514,430 , GRCh37.p13 chr9: 136,379,222-136,379,552 MYMK
    nsv5384438mobile element deletion1nstd186human GRCh37 chr9: 136,379,222-136,379,552 , GRCh38.p12 chr9: 133,514,100-133,514,430 MYMK
    nsv5383289mobile element deletion1nstd186human GRCh37 chr9: 136,379,198-136,379,551 , GRCh38.p12 chr9: 133,514,076-133,514,429 MYMK
    nsv5306220copy number variation1nstd204human GRCh37.p13 chr9: 136,369,183-136,539,282 , GRCh38.p13 chr9: 133,488,438-133,674,160 , DBH, 6 more genes
    nsv5220306mobile element deletion1nstd204human GRCh38.p13 chr9: 133,514,100-133,514,430 , GRCh37.p13 chr9: 136,379,222-136,379,552 MYMK
    nsv4985822copy number variation1nstd200human GRCh38 chr9: 133,524,633-133,694,233 , GRCh37.p13 chr9: 136,389,755-136,559,355 , ADAMTSL2, 5 more genes
    nsv4985821copy number variation1nstd200human GRCh38 chr9: 133,485,378-133,544,184 , GRCh37.p13 chr9: 136,369,193-136,409,306 ADAMTSL2, MYMK, 1 more genes
    nsv4893509mobile element deletion1nstd200human GRCh38 chr9: 133,514,100-133,514,430 , GRCh37.p13 chr9: 136,379,222-136,379,552 MYMK
    nsv4842905copy number variation1nstd200human GRCh37 chr9: 136,389,755-136,559,355 , GRCh38.p12 chr9: 133,524,633-133,694,233 , DBH-AS1, 5 more genes
    nsv4841884copy number variation1nstd200human GRCh37 chr9: 136,350,500-136,409,306 , GRCh38.p12 chr9: 133,485,378-133,544,184 LOC102723855, MYMK, 1 more genes
    nsv4831273copy number variation1nstd200human GRCh37 chr9: 136,353,569-136,539,274 , GRCh38.p12 chr9: 133,488,447-133,674,152 , DBH-AS1, 6 more genes
    nsv4771314mobile element deletion1nstd200human GRCh37 chr9: 136,379,197-136,379,552 , GRCh38.p12 chr9: 133,514,075-133,514,430 MYMK
    nsv4742640copy number variation1nstd199human GRCh37 chr9: 136,379,213-136,379,557 , GRCh38.p12 chr9: 133,514,091-133,514,435 MYMK
    nsv4702438copy number variation4nstd195human GRCh37 chr9: 136,379,210-136,379,211 , GRCh38.p12 chr9: 133,514,088-133,514,089 MYMK
    nsv4683889copy number variation1nstd102humanUncertain significance GRCh37 chr9: 135,771,850-137,038,881 , GRCh38.p12 chr9: 132,896,463-134,173,759 GBGT1, CELP, 46 more genes
    nsv4681357copy number variation1nstd102humanUncertain significance GRCh37 chr9: 135,771,602-136,769,889 , GRCh38.p12 chr9: 132,896,215-133,904,767 ABO, GTF3C5, 40 more genes
    nsv4635440mobile element deletion1nstd186human GRCh37 chr9: 136,379,211-136,379,552 , GRCh38.p12 chr9: 133,514,089-133,514,430 MYMK
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
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