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Items: 1 to 20 of 156

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112750copy number variation1nstd102humanPathogenic GRCh37 chr2: 81,209,244-86,688,030 , GRCh38.p12 chr2: 80,982,120-86,460,907 VAMP8, TMSB10, 86 more genes
    nsv5974407inversion1nstd209human GRCh38 chr2: 81,628,747-84,582,693 , GRCh37.p13 chr2: 81,855,871-84,809,817 DHFRP3, DNAH6, 24 more genes
    nsv5685087mobile element insertion1nstd211human GRCh38 chr2: 84,437,762-84,437,762 , GRCh37.p13 chr2: 84,664,886-84,664,886 SUCLG1
    nsv5673466copy number variation1nstd102humanPathogenic GRCh37 chr2: 84,650,850-84,686,413 , GRCh38.p12 chr2: 84,423,726-84,459,289 SUCLG1, DNAH6
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5449025copy number variation1nstd206human GRCh38 chr2: 84,452,576-84,456,617 , GRCh37.p13 chr2: 84,679,700-84,683,741 SUCLG1
    nsv5440126copy number variation1nstd206human GRCh38 chr2: 84,454,328-84,454,474 , GRCh37.p13 chr2: 84,681,452-84,681,598 SUCLG1
    nsv5360867translocation1nstd200human GRCh38 chr2: 84,456,617-84,456,617 , GRCh38 chr2: 84,452,576-84,452,576 , GRCh37.p13 chr2: 84,679,700-84,679,700 , GRCh37.p13 chr2: 84,683,741-84,683,741 SUCLG1
    nsv5345757translocation1nstd200human GRCh37 chr2: 84,683,741-84,683,741 , GRCh37 chr2: 84,679,700-84,679,700 , GRCh38.p12 chr2: 84,452,576-84,452,576 , GRCh38.p12 chr2: 84,456,617-84,456,617 SUCLG1
    nsv5288119copy number variation1nstd204human GRCh37.p13 chr2: 84,683,726-84,685,397 , GRCh38.p13 chr2: 84,456,602-84,458,273 DNAH6, SUCLG1
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4902329copy number variation1nstd200human GRCh38 chr2: 84,456,612-84,458,271 , GRCh37.p13 chr2: 84,683,736-84,685,395 SUCLG1, DNAH6
    nsv4902328copy number variation1nstd200human GRCh38 chr2: 84,446,093-84,446,240 , GRCh37.p13 chr2: 84,673,217-84,673,364 SUCLG1
    nsv4902304copy number variation1nstd200human GRCh38 chr2: 83,667,217-84,620,394 , GRCh37.p13 chr2: 83,894,341-84,847,518 DNAH6, SUCLG1, 4 more genes
    nsv4786623mobile element deletion1nstd200human GRCh37 chr2: 84,682,694-84,682,975 , GRCh38.p12 chr2: 84,455,570-84,455,851 SUCLG1
    nsv4776872copy number variation1nstd200human GRCh37 chr2: 84,673,217-84,673,364 , GRCh38.p12 chr2: 84,446,093-84,446,240 SUCLG1
    nsv4776855copy number variation1nstd200human GRCh37 chr2: 83,894,341-84,847,518 , GRCh38.p12 chr2: 83,667,217-84,620,394 DNAH6, SUCLG1, 4 more genes
    nsv4728322copy number variation1nstd102humanUncertain significance GRCh37 chr2: 83,598,955-84,683,243 , GRCh38.p12 chr2: 83,371,831-84,456,119 FUNDC2P2, RNU6-1312P, 7 more genes
    nsv4586571copy number variation1nstd183human GRCh37 chr2: 84,443,127-84,709,215 , GRCh38.p12 chr2: 84,216,003-84,482,091 DNAH6, SUCLG1, 2 more genes
    nsv4584592copy number variation1nstd183human GRCh37 chr2: 84,679,588-84,683,640 , GRCh38.p12 chr2: 84,452,464-84,456,516 SUCLG1
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