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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096653copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,121,051-47,710,088 , GRCh38.p12 chr2: 37,893,908-47,482,949 PLEKHH2, RNU6-566P, 151 more genes
    nsv7041290inversion1nstd229human GRCh38 chr2: 41,299,652-42,501,090 , GRCh37.p13 chr2: 41,526,792-42,728,230 RPS13P3, EML4-AS1, 15 more genes
    nsv7039759inversion1nstd229human GRCh38 chr2: 39,986,388-47,339,194 , GRCh37.p13 chr2: 40,213,528-47,566,333 RPL36AP14, CRIPT, 105 more genes
    nsv6673858copy number variation1nstd229human GRCh38 chr2: 42,473,854-42,489,673 , GRCh37.p13 chr2: 42,700,994-42,716,813 KCNG3
    nsv6673502copy number variation1nstd229human GRCh38 chr2: 42,415,701-42,721,700 , GRCh37.p13 chr2: 42,642,841-42,948,840 VDAC1P13, MTA3, 4 more genes
    nsv6672145copy number variation1nstd229human GRCh38 chr2: 42,392,538-42,558,773 , GRCh37.p13 chr2: 42,619,678-42,785,913 RPS13P3, KCNG3, 2 more genes
    nsv6663668copy number variation1nstd229human GRCh38 chr2: 42,448,852-42,457,810 , GRCh37.p13 chr2: 42,675,992-42,684,950 KCNG3
    nsv6662807copy number variation1nstd229human GRCh38 chr2: 42,492,601-42,494,800 , GRCh37.p13 chr2: 42,719,741-42,721,940 MTA3, KCNG3
    nsv6660549copy number variation1nstd229human GRCh38 chr2: 42,436,307-42,440,568 , GRCh37.p13 chr2: 42,663,447-42,667,708 KCNG3
    nsv6659562copy number variation1nstd229human GRCh38 chr2: 42,457,707-42,458,533 , GRCh37.p13 chr2: 42,684,847-42,685,673 KCNG3
    nsv6658391copy number variation1nstd229human GRCh38 chr2: 42,288,901-43,411,600 , GRCh37.p13 chr2: 42,516,041-43,638,739 LOC112268413, RNU6-958P, 22 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
    nsv6548072inversion1nstd223human GRCh38 chr2: 32,866,995-42,468,982 , GRCh37.p13 chr2: 33,092,062-42,696,122 PKDCC, SRSF7, 127 more genes
    nsv6544319inversion1nstd223human GRCh38 chr2: 42,466,489-42,467,087 , GRCh37.p13 chr2: 42,693,629-42,694,227 KCNG3
    nsv6542757inversion1nstd223human GRCh38 chr2: 32,866,974-42,451,061 , GRCh37.p13 chr2: 33,092,041-42,678,201 RASGRP3, TTC39DP, 125 more genes
    nsv6539485inversion1nstd223human GRCh38 chr2: 32,866,964-42,766,565 , GRCh37.p13 chr2: 33,092,031-42,993,705 RN7SL602P, RNU6-851P, 132 more genes
    nsv6338671copy number variation1nstd223human GRCh38 chr2: 42,484,360-42,536,373 , GRCh37.p13 chr2: 42,711,500-42,763,513 KCNG3, MTA3
    nsv6338299copy number variation1nstd223human GRCh38 chr2: 42,459,932-42,460,307 , GRCh37.p13 chr2: 42,687,072-42,687,447 KCNG3
    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
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