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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098844copy number variation1nstd102humanUncertain significance GRCh37 chr2: 65,296,579-71,305,638 , GRCh38.p12 chr2: 65,069,445-71,078,508 SNRNP27, TEX261, 121 more genes
    nsv7096520copy number variation1nstd102humanUncertain significance GRCh37 chr2: 69,240,632-74,779,761 , GRCh38.p12 chr2: 69,013,500-74,552,634 LOC112268419, DQX1, 140 more genes
    nsv7052045inversion1nstd229human GRCh38 chr2: 70,738,279-70,738,310 , GRCh37.p13 chr2: 70,965,411-70,965,442 , GRCh37.p13 chr2|NW_004504299.1: 304,561-304,592 ADD2
    nsv7052037inversion1nstd229human GRCh38 chr2: 69,732,002-70,868,430 , GRCh37.p13 chr2: 69,959,134-70,660,850 PCYOX1, FAM136A, 30 more genes
    nsv7043199inversion1nstd229human GRCh38 chr2: 70,623,217-71,162,741 , GRCh37.p13 chr2|NW_004504299.1: 189,499-599,580 , GRCh37.p13 chr2: 70,850,349-71,260,429 LOC105374796, MCEE, 22 more genes
    nsv7042226inversion1nstd229human GRCh38 chr2: 69,994,280-70,959,896 , GRCh37.p13 chr2|NW_004504299.1: 1-526,177 , GRCh37.p13 chr2: 70,660,851-71,187,026 PCBP1-AS1, SNRPG, 28 more genes
    nsv6675871copy number variation1nstd229human GRCh38 chr2: 70,723,107-70,727,792 , GRCh37.p13 chr2|NW_004504299.1: 289,389-294,074 , GRCh37.p13 chr2: 70,950,239-70,954,924 ADD2
    nsv6674288copy number variation1nstd229human GRCh38 chr2: 70,761,799-70,765,122 , GRCh37.p13 chr2|NW_004504299.1: 328,081-331,404 , GRCh37.p13 chr2: 70,988,931-70,992,254 ADD2
    nsv6673822copy number variation1nstd229human GRCh38 chr2: 70,761,555-70,765,205 , GRCh37.p13 chr2|NW_004504299.1: 327,837-331,487 , GRCh37.p13 chr2: 70,988,687-70,992,337 ADD2
    nsv6673263copy number variation1nstd229human GRCh38 chr2: 70,767,524-70,767,560 , GRCh37.p13 chr2|NW_004504299.1: 333,806-333,842 , GRCh37.p13 chr2: 70,994,656-70,994,692 ADD2
    nsv6672346copy number variation1nstd229human GRCh38 chr2: 70,761,446-70,765,201 , GRCh37.p13 chr2: 70,988,578-70,992,333 , GRCh37.p13 chr2|NW_004504299.1: 327,728-331,483 ADD2
    nsv6669871copy number variation1nstd229human GRCh38 chr2: 70,732,301-70,738,500 , GRCh37.p13 chr2|NW_004504299.1: 298,583-304,782 , GRCh37.p13 chr2: 70,959,433-70,965,632 ADD2
    nsv6667858copy number variation1nstd229human GRCh38 chr2: 70,726,787-70,732,458 , GRCh37.p13 chr2|NW_004504299.1: 293,069-298,740 , GRCh37.p13 chr2: 70,953,919-70,959,590 ADD2
    nsv6666830copy number variation1nstd229human GRCh38 chr2: 70,707,201-70,708,500 , GRCh37.p13 chr2|NW_004504299.1: 273,483-274,782 , GRCh37.p13 chr2: 70,934,333-70,935,632 ADD2
    nsv6666352copy number variation1nstd229human GRCh38 chr2: 70,698,401-70,702,000 , GRCh37.p13 chr2|NW_004504299.1: 264,683-268,282 , GRCh37.p13 chr2: 70,925,533-70,929,132 ADD2
    nsv6665681copy number variation1nstd229human GRCh38 chr2: 70,701,994-70,707,222 , GRCh37.p13 chr2: 70,929,126-70,934,354 , GRCh37.p13 chr2|NW_004504299.1: 268,276-273,504 ADD2
    nsv6665066copy number variation1nstd229human GRCh38 chr2: 70,761,401-70,764,200 , GRCh37.p13 chr2: 70,988,533-70,991,332 , GRCh37.p13 chr2|NW_004504299.1: 327,683-330,482 ADD2
    nsv6664179copy number variation1nstd229human GRCh38 chr2: 70,491,683-70,678,678 , GRCh37.p13 chr2: 70,718,815-70,905,810 , GRCh37.p13 chr2|NW_004504299.1: 57,965-244,960 TGFA, ADD2, 1 more genes
    nsv6663567copy number variation1nstd229human GRCh38 chr2: 70,728,026-70,728,232 , GRCh37.p13 chr2|NW_004504299.1: 294,308-294,514 , GRCh37.p13 chr2: 70,955,158-70,955,364 ADD2
    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
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