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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5869967copy number variation1nstd209human GRCh38 chr2: 100,572,304-100,572,609 , GRCh37.p13 chr2: 101,188,766-101,189,071 PDCL3
    nsv5721961mobile element insertion1nstd211human GRCh38 chr2: 100,576,352-100,576,352 , GRCh37.p13 chr2: 101,192,814-101,192,814 PDCL3
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5360934translocation1nstd200human GRCh38 chr2: 100,563,213-100,563,213 , GRCh38 chr2: 100,562,901-100,562,901 , GRCh37.p13 chr2: 101,179,675-101,179,675 , GRCh37.p13 chr2: 101,179,363-101,179,363 PDCL3
    nsv5299794copy number variation1nstd204human GRCh38.p13 chr2: 100,575,391-100,576,052 , GRCh37.p13 chr2: 101,191,853-101,192,514 PDCL3
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4894852copy number variation1nstd200human GRCh38 chr2: 100,570,592-100,571,307 , GRCh37.p13 chr2: 101,187,054-101,187,769 PDCL3
    nsv4894851copy number variation1nstd200human GRCh38 chr2: 100,564,302-100,565,580 , GRCh37.p13 chr2: 101,180,764-101,182,042 PDCL3
    nsv4894850copy number variation1nstd200human GRCh38 chr2: 100,561,334-100,576,048 , GRCh37.p13 chr2: 101,177,796-101,192,510 PDCL3
    nsv4894846copy number variation1nstd200human GRCh38 chr2: 100,201,568-100,618,404 , GRCh37.p13 chr2: 100,818,030-101,234,866 LONRF2, LINC01849, 9 more genes
    nsv4892917copy number variation1nstd200human GRCh38 chr2: 100,567,590-100,578,559 , GRCh37.p13 chr2: 101,184,052-101,195,021 PDCL3
    nsv4781670copy number variation1nstd200human GRCh37 chr2: 101,187,057-101,187,789 , GRCh38.p12 chr2: 100,570,595-100,571,327 PDCL3
    nsv4781669copy number variation1nstd200human GRCh37 chr2: 101,180,764-101,182,042 , GRCh38.p12 chr2: 100,564,302-100,565,580 PDCL3
    nsv4777186copy number variation1nstd200human GRCh37 chr2: 101,190,636-101,191,767 , GRCh38.p12 chr2: 100,574,174-100,575,305 PDCL3
    nsv4766632inversion1nstd199human GRCh37 chr2: 87,997,505-112,010,501 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,697,986-111,252,924 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 706 more genes
    nsv4752571inversion1nstd199human GRCh37 chr2: 87,550,795-112,295,517 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 87,323,672-111,537,940 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr9: 40,649,751-63,450,622 , ADRA2B, 723 more genes
    nsv4743379copy number variation1nstd199human GRCh37 chr2: 88,481,090-124,440,189 , GRCh38.p12 chr9: 40,649,751-63,450,622 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 88,181,571-123,682,613 , EIF2AK3, 861 more genes
    nsv4567215mobile element insertion1nstd166human GRCh37.p13 chr2: 101,192,088-101,192,088 , GRCh38.p12 chr2: 100,575,626-100,575,626 PDCL3
    nsv4366136copy number variation2nstd173human GRCh37 chr2: 101,152,837-101,206,166 , GRCh38.p12 chr2: 100,536,375-100,589,704 HMGN2P22, PDCL3
    nsv4312591inversion1nstd166human GRCh37.p13 chr2: 97,201,014-102,197,203 , GRCh38.p12 chr2: 96,535,277-101,580,741 , CNGA3, 106 more genes
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