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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137672copy number variation1nstd102humannot provided GRCh38 chr2: 124,348,648-129,410,245 , GRCh37.p13 chr2: 125,106,225-130,167,818 LOC105373603, MYO7B, 59 more genes
    nsv5968369inversion1nstd209human GRCh38 chr2: 127,459,348-127,614,077 , GRCh37.p13 chr2: 128,216,924-128,371,652 MYO7B, IWS1, 3 more genes
    nsv5964268insertion1nstd209human GRCh38 chr2: 127,571,442-127,571,442 , GRCh37.p13 chr2: 128,329,017-128,329,017 MYO7B, LOC105373609
    nsv5898222copy number variation1nstd209human GRCh38 chr2: 127,609,181-127,615,853 , GRCh37.p13 chr2: 128,366,756-128,373,428 MYO7B
    nsv5890051copy number variation1nstd209human GRCh38 chr2: 127,634,690-127,634,743 , GRCh37.p13 chr2: 128,392,265-128,392,318 MYO7B
    nsv5831253copy number variation2nstd209human GRCh38 chr2: 127,609,033-127,611,182 , GRCh37.p13 chr2: 128,366,608-128,368,757 MYO7B
    nsv5831219copy number variation1nstd209human GRCh38 chr2: 127,613,733-127,615,332 , GRCh37.p13 chr2: 128,371,308-128,372,907 MYO7B
    nsv5831218copy number variation1nstd209human GRCh38 chr2: 127,609,158-127,615,632 , GRCh37.p13 chr2: 128,366,733-128,373,207 MYO7B
    nsv5679083mobile element insertion1nstd211human GRCh38 chr2: 127,542,887-127,542,887 , GRCh37.p13 chr2: 128,300,462-128,300,462 MYO7B
    nsv5566768copy number variation1nstd207human GRCh38 chr2: 127,634,690-127,634,743 , GRCh37.p13 chr2: 128,392,265-128,392,318 MYO7B
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5443166copy number variation1nstd206human GRCh38 chr2: 127,632,773-127,632,845 , GRCh37.p13 chr2: 128,390,348-128,390,420 MYO7B
    nsv5441500copy number variation1nstd206human GRCh38 chr2: 127,617,489-127,617,800 , GRCh37.p13 chr2: 128,375,064-128,375,375 MYO7B
    nsv5436318copy number variation1nstd206human GRCh38 chr2: 127,566,140-127,578,709 , GRCh37.p13 chr2: 128,323,715-128,336,284 MYO7B, LOC105373609
    nsv5411278mobile element insertion1nstd206human GRCh38 chr2: 127,542,887-127,542,938 , GRCh37.p13 chr2: 128,300,462-128,300,513 MYO7B
    nsv5380654translocation1nstd200human GRCh38 chr2: 127,614,078-127,614,078 , GRCh38 chr2: 127,459,348-127,459,348 , GRCh37.p13 chr2: 128,216,924-128,216,924 , GRCh37.p13 chr2: 128,371,653-128,371,653 LOC105373608, MYO7B
    nsv5380653translocation1nstd200human GRCh38 chr2: 127,615,366-127,615,366 , GRCh38 chr2: 127,449,381-127,449,381 , GRCh37.p13 chr2: 128,372,941-128,372,941 , GRCh37.p13 chr2: 128,206,957-128,206,957 MYO7B, LOC105373608
    nsv5336389translocation1nstd200human GRCh37 chr2: 128,371,653-128,371,653 , GRCh37 chr2: 128,216,924-128,216,924 , GRCh38.p12 chr2: 127,614,078-127,614,078 , GRCh38.p12 chr2: 127,459,348-127,459,348 MYO7B, LOC105373608
    nsv5332744translocation1nstd200human GRCh37 chr2: 128,206,957-128,206,957 , GRCh37 chr2: 128,372,941-128,372,941 , GRCh38.p12 chr2: 127,449,381-127,449,381 , GRCh38.p12 chr2: 127,615,366-127,615,366 LOC105373608, MYO7B
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