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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5690639mobile element insertion1nstd211human GRCh38 chr2: 110,260,764-110,260,764 , GRCh37.p13 chr2: 111,018,341-111,018,341 LOC100507334
    nsv5670764inversion1nstd207human GRCh38 chr2: 110,095,328-110,276,209 , GRCh37.p13 chr2: 110,852,905-111,033,786 NPHP1, MALL, 3 more genes
    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
    nsv5444675copy number variation1nstd206human GRCh38 chr2: 110,047,618-110,274,704 , GRCh37.p13 chr2: 110,805,195-111,032,281 NPHP1, MALL, 6 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
    nsv5436824copy number variation1nstd206human GRCh38 chr2: 110,057,618-110,259,618 , GRCh37.p13 chr2: 110,815,195-111,017,195 NPHP1, MALL, 5 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
    nsv5217030copy number variation1nstd204human GRCh38.p13 chr2: 110,246,301-110,260,400 , GRCh37.p13 chr2: 111,003,878-111,017,977 LOC100507334
    nsv5216989copy number variation1nstd204human GRCh38.p13 chr2: 110,228,401-110,268,100 , GRCh37.p13 chr2: 110,985,978-111,025,677 MTLN, LOC100507334
    nsv5215226copy number variation1nstd204human GRCh38.p13 chr2: 110,253,801-110,255,400 , GRCh37.p13 chr2: 111,011,378-111,012,977 LOC100507334
    nsv5214398copy number variation1nstd204human GRCh38.p13 chr2: 110,229,201-110,275,800 , GRCh37.p13 chr2: 110,986,778-111,033,377 MTLN, LOC100507334
    nsv5213274copy number variation1nstd204human GRCh38.p13 chr2: 110,229,201-110,274,300 , GRCh37.p13 chr2: 110,986,778-111,031,877 MTLN, LOC100507334
    nsv5211279copy number variation1nstd204human GRCh38.p13 chr2: 110,253,801-110,268,000 , GRCh37.p13 chr2: 111,011,378-111,025,577 LOC100507334
    nsv5211170copy number variation1nstd204human GRCh38.p13 chr2: 110,253,801-110,258,800 , GRCh37.p13 chr2: 111,011,378-111,016,377 LOC100507334
    nsv5210473copy number variation1nstd204human GRCh38.p13 chr2: 110,227,701-110,263,600 , GRCh37.p13 chr2: 110,985,278-111,021,177 LOC100507334, MTLN
    nsv5209631copy number variation1nstd204human GRCh38.p13 chr2: 110,229,201-110,246,500 , GRCh37.p13 chr2: 110,986,778-111,004,077 LOC100507334, MTLN
    nsv5208112copy number variation1nstd204human GRCh38.p13 chr2: 110,251,801-110,273,300 , GRCh37.p13 chr2: 111,009,378-111,030,877 LOC100507334
    nsv5207876copy number variation1nstd204human GRCh38.p13 chr2: 110,229,201-110,247,700 , GRCh37.p13 chr2: 110,986,778-111,005,277 MTLN, LOC100507334
    nsv5207358copy number variation1nstd204human GRCh38.p13 chr2: 110,238,401-110,259,000 , GRCh37.p13 chr2: 110,995,978-111,016,577 LOC100507334, MTLN
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