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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5833718copy number variation2nstd209human GRCh38 chr2: 74,610,443-74,614,551 , GRCh37.p13 chr2: 74,837,570-74,841,678 M1AP
    nsv5677350mobile element insertion1nstd211human GRCh38 chr2: 74,641,075-74,641,075 , GRCh37.p13 chr2: 74,868,202-74,868,202 M1AP
    nsv5616380insertion2nstd207human GRCh38 chr2: 74,561,067-74,561,067 , GRCh37.p13 chr2: 74,788,194-74,788,194 M1AP
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5448527copy number variation1nstd206human GRCh38 chr2: 74,602,198-74,602,381 , GRCh37.p13 chr2: 74,829,325-74,829,508 M1AP
    nsv5440705copy number variation1nstd206human GRCh38 chr2: 74,560,968-74,562,003 , GRCh37.p13 chr2: 74,788,095-74,789,130 M1AP
    nsv5405162mobile element insertion1nstd206human GRCh38 chr2: 74,641,075-74,641,126 , GRCh37.p13 chr2: 74,868,202-74,868,253 M1AP
    nsv5360792translocation1nstd200human GRCh38 chr2: 74,593,750-74,593,750 , GRCh38 chr2: 74,596,917-74,596,917 , GRCh37.p13 chr2: 74,824,044-74,824,044 , GRCh37.p13 chr2: 74,820,877-74,820,877 M1AP
    nsv5194258mobile element insertion1nstd203human GRCh38 chr2: 74,616,443-74,616,458 , GRCh37.p13 chr2: 74,843,570-74,843,585 M1AP
    nsv5076074mobile element insertion1nstd203human GRCh38 chr2: 74,601,147-74,601,161 , GRCh37.p13 chr2: 74,828,274-74,828,288 M1AP
    nsv4908824copy number variation1nstd200human GRCh38 chr2: 74,602,198-74,602,381 , GRCh37.p13 chr2: 74,829,325-74,829,508 M1AP
    nsv4908823copy number variation1nstd200human GRCh38 chr2: 74,593,093-75,089,577 , GRCh37.p13 chr2: 74,820,220-75,316,704 , LOC105374809, 13 more genes
    nsv4901940copy number variation1nstd200human GRCh38 chr2: 74,640,882-74,643,712 , GRCh37.p13 chr2: 74,868,009-74,870,839 M1AP
    nsv4901939copy number variation1nstd200human GRCh38 chr2: 74,590,524-74,594,100 , GRCh37.p13 chr2: 74,817,651-74,821,227 M1AP
    nsv4901938copy number variation1nstd200human GRCh38 chr2: 74,587,312-74,594,100 , GRCh37.p13 chr2: 74,814,439-74,821,227 M1AP
    nsv4901937copy number variation1nstd200human GRCh38 chr2: 74,587,313-74,590,370 , GRCh37.p13 chr2: 74,814,440-74,817,497 M1AP
    nsv4781577copy number variation1nstd200human GRCh37 chr2: 74,829,325-74,829,508 , GRCh38.p12 chr2: 74,602,198-74,602,381 M1AP
    nsv4776586copy number variation1nstd200human GRCh37 chr2: 74,868,009-74,870,839 , GRCh38.p12 chr2: 74,640,882-74,643,712 M1AP
    nsv4776585copy number variation1nstd200human GRCh37 chr2: 74,817,651-74,821,227 , GRCh38.p12 chr2: 74,590,524-74,594,100 M1AP
    nsv4776584copy number variation1nstd200human GRCh37 chr2: 74,814,396-74,817,497 , GRCh38.p12 chr2: 74,587,269-74,590,370 M1AP
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