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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6636315copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 95,341,388-100,340,514 , GRCh38.p12 chr2: 94,675,663-99,724,052 ADRA2B, ATP5F1BP1, 130 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6628428copy number variation1nstd224human GRCh37 chr2: 96,423,982-96,690,279 , GRCh38.p12 chr2: 95,758,234-96,024,531 LINC00342, GPAT2, 4 more genes
    nsv6628427copy number variation1nstd224human GRCh37 chr2: 96,378,210-96,690,279 , GRCh38.p12 chr2: 95,712,462-96,024,531 LINC00342, GPAT2, 4 more genes
    nsv6628241copy number variation1nstd224human GRCh37 chr2: 96,378,210-96,672,001 , GRCh38.p12 chr2: 95,712,462-96,006,253 ANKRD36C, LINC00342, 2 more genes
    nsv6628240copy number variation1nstd224human GRCh37 chr2: 96,195,730-96,690,279 , GRCh38.p12 chr2: 95,529,982-96,024,531 OR7E102P, FAHD2CP, 13 more genes
    nsv6628178copy number variation4nstd224human GRCh37 chr2: 96,465,201-96,580,165 , GRCh38.p12 chr2: 95,799,453-95,914,417 ANKRD36C, GPAT2P1, 1 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6313735copy number variation1nstd102humanUncertain significance GRCh37 chr2: 95,341,387-96,735,978 , GRCh38.p12 chr2: 94,675,662-96,070,230 TRIM43, SNX18P14, 48 more genes
    nsv6134374copy number variation1nstd213human GRCh37 chr2: 95,650,000-97,860,001 , GRCh38.p12 chr2: 94,984,255-97,194,264 ADRA2B, DUSP2, 68 more genes
    nsv6105281inversion1nstd212human GRCh38 chr2: 95,666,674-95,918,762 , GRCh37.p13 chr2: 96,332,422-96,584,510 , LINC00342, 3 more genes
    nsv6104368inversion1nstd212human GRCh38 chr2: 95,752,382-96,071,259 , GRCh37.p13 chr2: 96,418,130-96,737,007 , LINC00342, 7 more genes
    nsv5990662copy number variation1nstd212human GRCh38 chr2: 95,820,573-95,825,675 , GRCh37.p13 chr2: 96,486,321-96,491,423 LINC00342
    nsv5973264inversion1nstd209human GRCh38 chr2: 95,666,673-95,918,761 , GRCh37.p13 chr2: 96,332,421-96,584,509 , LINC00342, 3 more genes
    nsv5880065copy number variation1nstd209human GRCh38 chr2: 95,820,572-95,825,674 , GRCh37.p13 chr2: 96,486,320-96,491,422 LINC00342
    nsv5870935copy number variation1nstd209human GRCh38 chr2: 95,800,608-95,824,160 , GRCh37.p13 chr2: 96,466,356-96,489,908 LINC00342, GPAT2P1
    nsv5834450copy number variation2nstd209human GRCh38 chr2: 95,820,571-95,826,015 , GRCh37.p13 chr2: 96,486,319-96,491,763 LINC00342
    nsv5834449copy number variation2nstd209human GRCh38 chr2: 95,795,512-95,824,792 , GRCh37.p13 chr2: 96,461,260-96,490,540 LINC00342, GPAT2P1
    nsv5665155inversion1nstd207human GRCh38 chr2: 95,801,271-96,023,342 , GRCh37.p13 chr2: 96,467,019-96,689,090 LINC00342, GPAT2, 3 more genes
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