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Items: 1 to 20 of 328

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6130884insertion1nstd186human GRCh37 chr21: 10,697,897-44,966,043 , GRCh38.p12 chr21: 12,965,809-43,546,162 , APP, 533 more genes
    nsv6129414insertion1nstd186human GRCh37 chr21: 33,045,784-33,045,784 , GRCh38.p12 chr21: 31,673,471-31,673,471 SCAF4
    nsv6117003mobile element insertion1nstd186human GRCh37 chr21: 33,050,849-33,050,900 , GRCh38.p12 chr21: 31,678,536-31,678,587 SCAF4
    nsv5973550insertion1nstd209human GRCh38 chr21: 31,688,114-31,688,114 , GRCh37.p13 chr21: 33,060,427-33,060,427 SCAF4
    nsv5969347insertion1nstd209human GRCh38 chr21: 31,673,471-31,673,471 , GRCh37.p13 chr21: 33,045,784-33,045,784 SCAF4
    nsv5968609insertion1nstd209human GRCh38 chr21: 31,678,520-31,678,520 , GRCh37.p13 chr21: 33,050,833-33,050,833 SCAF4
    nsv5699298mobile element insertion2nstd211human GRCh38 chr21: 31,678,536-31,678,536 , GRCh37.p13 chr21: 33,050,849-33,050,849 SCAF4
    nsv5665477insertion1nstd207human GRCh38 chr21: 31,673,471-31,673,471 , GRCh37.p13 chr21: 33,045,784-33,045,784 SCAF4
    nsv5547941copy number variation1nstd206human GRCh38 chr21: 31,724,239-31,724,344 , GRCh37.p13 chr21: 33,096,552-33,096,657 SCAF4
    nsv5539790insertion1nstd206human GRCh38 chr21: 5,227,438-39,583,816 , GRCh37.p13 chr21: 10,697,897-44,966,043 , LOC100419041, 557 more genes
    nsv5536592insertion1nstd206human GRCh38 chr21: 31,673,471-31,673,471 , GRCh37.p13 chr21: 33,045,784-33,045,784 SCAF4
    nsv5422538mobile element insertion1nstd206human GRCh38 chr21: 31,678,536-31,678,587 , GRCh37.p13 chr21: 33,050,849-33,050,900 SCAF4
    nsv5381310copy number variation1nstd102humanUncertain significance GRCh37 chr21: 32,439,271-37,133,458 , GRCh38.p12 chr21: 31,066,952-35,761,160 LINC00945, CFAP298-TCP10L, 83 more genes
    nsv5341229translocation1nstd200human GRCh37 chr21: 33,096,121-33,096,121 , GRCh37 chr21: 33,099,707-33,099,707 , GRCh38.p12 chr21: 31,723,808-31,723,808 , GRCh38.p12 chr21: 31,727,394-31,727,394 SCAF4
    nsv5324608translocation1nstd204human GRCh38.p13 chr21: 31,723,808-31,723,808 , GRCh38.p13 chr21: 31,727,394-31,727,394 , GRCh37.p13 chr21: 33,096,121-33,096,121 , GRCh37.p13 chr21: 33,099,707-33,099,707 SCAF4
    nsv5323906inversion1nstd204human GRCh37.p13 chr21: 30,417,326-35,280,637 , GRCh38.p13 chr21: 29,045,005-33,908,333 , ATP5PO, 129 more genes
    nsv5176224mobile element insertion1nstd203human GRCh38 chr21: 31,678,527-31,678,536 , GRCh37.p13 chr21: 33,050,840-33,050,849 SCAF4
    nsv5175411mobile element insertion1nstd203human GRCh38 chr21: 31,678,524-31,678,536 , GRCh37.p13 chr21: 33,050,837-33,050,849 SCAF4
    nsv5171829mobile element insertion1nstd203human GRCh38 chr21: 31,688,114-31,688,145 , GRCh37.p13 chr21: 33,060,427-33,060,458 SCAF4
    nsv5169523mobile element insertion1nstd203human GRCh38 chr21: 31,678,520-31,678,536 , GRCh37.p13 chr21: 33,050,833-33,050,849 SCAF4
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