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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096920copy number variation1nstd102humanPathogenic GRCh37 chr2: 86,479,060-86,481,957 , GRCh38.p12 chr2: 86,251,937-86,254,834 REEP1
    nsv7096919copy number variation1nstd102humanUncertain significance GRCh37 chr2: 86,459,728-86,459,945 , GRCh38.p12 chr2: 86,232,605-86,232,822 REEP1
    nsv7096678copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 86,479,060-86,509,385 , GRCh38.p12 chr2: 86,251,937-86,282,262 REEP1
    nsv7096524copy number variation1nstd102humanPathogenic GRCh37 chr2: 85,766,411-86,564,633 , GRCh38.p12 chr2: 85,539,288-86,337,510 GPR160P1, USP39, 27 more genes
    nsv7093366copy number variation1nstd102humanUncertain significance GRCh37 chr2: 86,292,397-86,509,365 , GRCh38.p12 chr2: 86,065,274-86,282,242 SNORD94, REEP1, 5 more genes
    nsv7053780inversion1nstd229human GRCh38 chr2: 86,231,921-86,232,032 , GRCh37.p13 chr2: 86,459,044-86,459,155 REEP1
    nsv7049583inversion1nstd229human GRCh38 chr2: 86,257,520-86,257,576 , GRCh37.p13 chr2: 86,484,643-86,484,699 REEP1
    nsv7040710inversion1nstd229human GRCh38 chr2: 86,335,101-86,335,180 , GRCh37.p13 chr2: 86,562,224-86,562,303 REEP1
    nsv6696147copy number variation1nstd229human GRCh38 chr2: 86,292,035-86,308,742 , GRCh37.p13 chr2: 86,519,158-86,535,865 REEP1
    nsv6694445copy number variation1nstd229human GRCh38 chr2: 86,334,142-86,337,356 , GRCh37.p13 chr2: 86,561,265-86,564,479 REEP1
    nsv6692985copy number variation1nstd229human GRCh38 chr2: 86,284,277-86,286,701 , GRCh37.p13 chr2: 86,511,400-86,513,824 REEP1
    nsv6690771copy number variation1nstd229human GRCh38 chr2: 86,255,557-86,259,105 , GRCh37.p13 chr2: 86,482,680-86,486,228 REEP1
    nsv6690436copy number variation1nstd229human GRCh38 chr2: 86,277,101-86,279,800 , GRCh37.p13 chr2: 86,504,224-86,506,923 REEP1
    nsv6690292copy number variation1nstd229human GRCh38 chr2: 86,151,038-86,226,591 , GRCh37.p13 chr2: 86,378,161-86,453,714 MIR4779, IMMT, 2 more genes
    nsv6687440copy number variation1nstd229human GRCh38 chr2: 86,235,275-86,245,079 , GRCh37.p13 chr2: 86,462,398-86,472,202 REEP1
    nsv6686085copy number variation1nstd229human GRCh38 chr2: 86,269,001-86,272,700 , GRCh37.p13 chr2: 86,496,124-86,499,823 REEP1
    nsv6681757copy number variation1nstd229human GRCh38 chr2: 86,335,886-86,335,954 , GRCh37.p13 chr2: 86,563,009-86,563,077 REEP1
    nsv6680780copy number variation1nstd229human GRCh38 chr2: 86,055,590-86,283,810 , GRCh37.p13 chr2: 86,282,713-86,510,933 SNORD94, PTCD3, 5 more genes
    nsv6680082copy number variation1nstd229human GRCh38 chr2: 86,226,394-86,226,456 , GRCh37.p13 chr2: 86,453,517-86,453,579 REEP1
    nsv6636862copy number variation1nstd102humanUncertain significance GRCh37 chr2: 85,786,007-86,559,358 , GRCh38.p12 chr2: 85,558,884-86,332,235 MIR4779, RN7SKP83, 25 more genes
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