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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056098inversion1nstd229human GRCh38 chr2: 110,207,154-110,365,768 , GRCh37.p13 chr2: 110,964,731-111,123,345 MTLN, LOC105373551, 5 more genes
    nsv7052468inversion1nstd229human GRCh38 chr2: 109,726,921-110,637,321 , GRCh37.p13 chr2: 110,484,498-111,394,898 LOC105373553, NPHP1, 39 more genes
    nsv6686545copy number variation1nstd229human GRCh38 chr2: 103,585,907-110,943,040 , GRCh37.p13 chr2: 104,202,365-111,700,617 PPP1R2P5, CAPZBP1, 142 more genes
    nsv6634363copy number variation1nstd102humanUncertain significance GRCh37 chr2: 110,498,141-111,365,996 , GRCh38.p12 chr2: 109,740,564-110,608,419 NPHP1, MIR4436B1, 34 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
    nsv6353324copy number variation1nstd223human GRCh38 chr2: 110,328,601-110,331,000 , GRCh37.p13 chr2: 111,086,178-111,088,577 LOC105373551
    nsv6315445copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr2: 110,504,318-111,365,996 , GRCh38.p12 chr2: 109,746,741-110,608,419 LOC107985776, LOC105375809, 34 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
    nsv6139401copy number variation1nstd206human GRCh38 chr2: 110,321,784-110,415,118 , GRCh37.p13 chr2: 111,079,361-111,172,695 LINC01106, LOC442041, 7 more genes
    nsv5985309copy number variation1nstd212human GRCh38 chr2: 108,715,210-112,293,808 , GRCh37.p13 chr2: 109,331,666-113,051,385 , NPHP1, 85 more genes
    nsv5874658copy number variation1nstd209human GRCh38 chr2: 110,334,789-110,334,877 , GRCh37.p13 chr2: 111,092,366-111,092,454 LOC107985776, LOC105373551
    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
    nsv5442426copy number variation1nstd206human GRCh38 chr2: 109,913,618-110,441,618 , GRCh37.p13 chr2: 110,671,195-111,199,195 LIMS3-LOC440895, LOC105373547, 28 more genes
    nsv5435652copy number variation1nstd206human GRCh38 chr2: 110,323,618-110,440,200 , GRCh37.p13 chr2: 111,081,195-111,197,777 LINC01106, LOC442041, 7 more genes
    nsv5435509copy number variation1nstd206human GRCh38 chr2: 109,743,550-110,910,000 , GRCh37.p13 chr2: 110,501,127-111,667,577 MIR4436B2, LOC112268438, 40 more genes
    nsv5219290copy number variation1nstd204human GRCh38.p13 chr2: 110,326,301-110,328,200 , GRCh37.p13 chr2: 111,083,878-111,085,777 LOC105373551
    nsv5218707copy number variation1nstd204human GRCh38.p13 chr2: 110,333,601-110,334,200 , GRCh37.p13 chr2: 111,091,178-111,091,777 LOC107985776, LOC105373551
    nsv5214210copy number variation1nstd204human GRCh38.p13 chr2: 110,327,101-110,328,200 , GRCh37.p13 chr2: 111,084,678-111,085,777 LOC105373551
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