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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5903501copy number variation1nstd209human GRCh38 chr2: 240,054,142-240,054,223 , GRCh37.p13 chr2: 240,993,559-240,993,640 OR6B3
    nsv5582323copy number variation1nstd207human GRCh38 chr2: 240,042,551-240,042,662 , GRCh37.p13 chr2: 240,981,968-240,982,079 OR6B3
    nsv5580975copy number variation1nstd207human GRCh38 chr2: 240,054,142-240,054,223 , GRCh37.p13 chr2: 240,993,559-240,993,640 OR6B3
    nsv5572793copy number variation1nstd207human GRCh38 chr2: 240,042,131-240,042,634 , GRCh37.p13 chr2: 240,981,548-240,982,051 OR6B3
    nsv5448614copy number variation1nstd206human GRCh38 chr2: 240,054,145-240,054,224 , GRCh37.p13 chr2: 240,993,562-240,993,641 OR6B3
    nsv5445465copy number variation1nstd206human GRCh38 chr2: 240,030,023-240,046,047 , GRCh37.p13 chr2: 240,969,440-240,985,464 OR6B3, OR6B2
    nsv5441752copy number variation1nstd206human GRCh38 chr2: 240,042,083-240,042,726 , GRCh37.p13 chr2: 240,981,500-240,982,143 OR6B3
    nsv5438323copy number variation1nstd206human GRCh38 chr2: 240,042,968-240,049,892 , GRCh37.p13 chr2: 240,982,385-240,989,309 OR6B3
    nsv5389130copy number variation1nstd186human GRCh37 chr2: 240,981,426-240,982,037 , GRCh38.p12 chr2: 240,042,009-240,042,620 OR6B3
    nsv5381323copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,201,756-243,048,760 , GRCh38.p12 chr2: 236,293,113-242,106,609 LRRFIP1, GPR35, 133 more genes
    nsv5351279translocation1nstd200human GRCh38 chr2: 240,054,145-240,054,145 , GRCh38 chr2: 240,054,224-240,054,224 , GRCh37.p13 chr2: 240,993,641-240,993,641 , GRCh37.p13 chr2: 240,993,562-240,993,562 OR6B3
    nsv5343381translocation1nstd200human GRCh37 chr2: 240,993,641-240,993,641 , GRCh37 chr2: 240,993,562-240,993,562 , GRCh38.p12 chr2: 240,054,145-240,054,145 , GRCh38.p12 chr2: 240,054,224-240,054,224 OR6B3
    nsv5327223translocation1nstd204human GRCh38.p13 chr2: 240,054,145-240,054,145 , GRCh38.p13 chr2: 240,054,224-240,054,224 , GRCh37.p13 chr2: 240,993,562-240,993,562 , GRCh37.p13 chr2: 240,993,641-240,993,641 OR6B3
    nsv5209960copy number variation1nstd204human GRCh38.p13 chr2: 240,042,101-240,042,700 , GRCh37.p13 chr2: 240,981,518-240,982,117 OR6B3
    nsv5200340copy number variation1nstd102humanPathogenic GRCh37 chr2: 239,860,877-241,385,960 , GRCh38.p12 chr2: 238,939,181-240,446,543 MIR4269, LOC102723825, 20 more genes
    nsv4914134copy number variation1nstd200human GRCh38 chr2: 239,634,255-240,249,262 , GRCh37.p13 chr2: 240,555,949-241,188,679 OTOS, LOC150935, 9 more genes
    nsv4910408copy number variation1nstd200human GRCh38 chr2: 240,042,968-240,049,892 , GRCh37.p13 chr2: 240,982,385-240,989,309 OR6B3
    nsv4910407copy number variation1nstd200human GRCh38 chr2: 240,042,006-240,042,678 , GRCh37.p13 chr2: 240,981,423-240,982,095 OR6B3
    nsv4804729copy number variation1nstd200human GRCh37 chr2: 240,555,949-241,188,679 , GRCh38.p12 chr2: 239,634,255-240,249,262 OR6B2, OTOS, 9 more genes
    nsv4768328copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,110,452-243,028,452 , GRCh38.p12 chr2: 232,245,742-242,086,301 LOC107985836, LOC105373980, 217 more genes
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