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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5888921copy number variation1nstd209human GRCh38 chr2: 237,401,367-237,406,686 , GRCh37.p13 chr2: 238,310,010-238,315,329 COL6A3
    nsv5832571copy number variation1nstd209human GRCh38 chr2: 237,401,308-237,406,971 , GRCh37.p13 chr2: 238,309,951-238,315,614 COL6A3
    nsv5832570copy number variation2nstd209human GRCh38 chr2: 237,341,250-237,343,881 , GRCh37.p13 chr2: 238,249,893-238,252,524 COL6A3
    nsv5673218copy number variation1nstd102humanPathogenic GRCh37 chr2: 237,481,970-238,305,470 , GRCh38.p12 chr2: 236,573,327-237,396,827 LOC105373946, LOC105373949, 13 more genes
    nsv5619890insertion1nstd207human GRCh38 chr2: 237,427,373-237,427,373 , GRCh37.p13 chr2: 238,336,016-238,336,016 COL6A3
    nsv5448313copy number variation1nstd206human GRCh38 chr2: 237,401,367-237,406,687 , GRCh37.p13 chr2: 238,310,010-238,315,330 COL6A3
    nsv5446961copy number variation1nstd206human GRCh38 chr2: 237,432,797-237,437,577 , GRCh37.p13 chr2: 238,341,440-238,346,220 COL6A3
    nsv5437199copy number variation1nstd206human GRCh38 chr2: 237,339,346-237,339,520 , GRCh37.p13 chr2: 238,247,989-238,248,163 COL6A3
    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
    nsv5381247copy number variation1nstd102humanUncertain significance GRCh37 chr2: 238,242,073-238,243,552 , GRCh38.p12 chr2: 237,333,430-237,334,909 COL6A3
    nsv5381170copy number variation1nstd102humanUncertain significance GRCh37 chr2: 238,233,407-238,305,470 , GRCh38.p12 chr2: 237,324,764-237,396,827 COL6A3
    nsv5309358copy number variation1nstd204human GRCh38.p13 chr2: 237,314,858-237,330,598 , GRCh37.p13 chr2: 238,223,501-238,239,241 COL6A3
    nsv5307727copy number variation1nstd204human GRCh38.p13 chr2: 237,412,624-237,464,400 , GRCh37.p13 chr2: 238,321,267-238,373,043 COL6A3
    nsv5307333copy number variation1nstd204human GRCh38.p13 chr2: 237,401,367-237,406,687 , GRCh37.p13 chr2: 238,310,010-238,315,330 COL6A3
    nsv5219754copy number variation1nstd204human GRCh38.p13 chr2: 237,412,601-237,464,400 , GRCh37.p13 chr2: 238,321,244-238,373,043 COL6A3
    nsv5215373copy number variation1nstd204human GRCh38.p13 chr2: 237,340,900-237,345,131 , GRCh37.p13 chr2: 238,249,543-238,253,774 COL6A3
    nsv5215104copy number variation1nstd204human GRCh38.p13 chr2: 237,411,864-237,445,973 , GRCh37.p13 chr2: 238,320,507-238,354,616 COL6A3
    nsv5213441copy number variation1nstd204human GRCh38.p13 chr2: 237,401,401-237,409,200 , GRCh37.p13 chr2: 238,310,044-238,317,843 COL6A3
    nsv5211969copy number variation1nstd204human GRCh38.p13 chr2: 237,412,664-237,424,276 , GRCh37.p13 chr2: 238,321,307-238,332,919 COL6A3
    nsv5207301copy number variation1nstd204human GRCh38.p13 chr2: 237,401,371-237,406,403 , GRCh37.p13 chr2: 238,310,014-238,315,046 COL6A3
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