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Items: 1 to 20 of 763

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980034inversion1nstd209human GRCh38 chr3: 83,154,897-85,212,825 , GRCh37.p13 chr3: 83,204,048-85,261,975 CADM2, LINC00971, 11 more genes
    nsv5966294insertion1nstd209human GRCh38 chr3: 84,868,040-84,868,040 , GRCh37.p13 chr3: 84,917,191-84,917,191 LINC00971
    nsv5962451insertion1nstd209human GRCh38 chr3: 84,775,262-84,775,262 , GRCh37.p13 chr3: 84,824,413-84,824,413 LINC00971
    nsv5947954insertion1nstd209human GRCh38 chr3: 84,782,968-84,782,968 , GRCh37.p13 chr3: 84,832,119-84,832,119 LINC00971
    nsv5897129copy number variation1nstd209human GRCh38 chr3: 84,650,369-84,653,709 , GRCh37.p13 chr3: 84,699,520-84,702,860 LINC00971
    nsv5891734copy number variation1nstd209human GRCh38 chr3: 84,650,179-84,653,726 , GRCh37.p13 chr3: 84,699,330-84,702,877 LINC00971
    nsv5888502copy number variation1nstd209human GRCh38 chr3: 84,695,294-84,695,390 , GRCh37.p13 chr3: 84,744,445-84,744,541 LINC00971
    nsv5836860copy number variation1nstd209human GRCh38 chr3: 84,650,459-84,653,558 , GRCh37.p13 chr3: 84,699,610-84,702,709 LINC00971
    nsv5692771mobile element insertion1nstd211human GRCh38 chr3: 84,796,363-84,796,363 , GRCh37.p13 chr3: 84,845,514-84,845,514 LINC00971
    nsv5686722mobile element insertion2nstd211human GRCh38 chr3: 84,782,982-84,782,982 , GRCh37.p13 chr3: 84,832,133-84,832,133 LINC00971
    nsv5680396mobile element insertion1nstd211human GRCh38 chr3: 84,679,611-84,679,611 , GRCh37.p13 chr3: 84,728,762-84,728,762 LINC00971
    nsv5678151mobile element insertion2nstd211human GRCh38 chr3: 84,683,057-84,683,057 , GRCh37.p13 chr3: 84,732,208-84,732,208 LINC00971
    nsv5605197insertion1nstd207human GRCh38 chr3: 84,782,968-84,782,968 , GRCh37.p13 chr3: 84,832,119-84,832,119 LINC00971
    nsv5574462copy number variation1nstd207human GRCh38 chr3: 84,650,419-84,653,777 , GRCh37.p13 chr3: 84,699,570-84,702,928 LINC00971
    nsv5561554mobile element insertion1nstd206human GRCh38 chr3: 84,713,054-84,713,054 , GRCh37.p13 chr3: 84,762,205-84,762,205 LINC00971
    nsv5559506sequence alteration1nstd206human GRCh38 chr3: 84,817,387-84,822,760 , GRCh37.p13 chr3: 84,866,538-84,871,911 LINC00971
    nsv5446691copy number variation1nstd206human GRCh38 chr3: 84,664,959-84,665,016 , GRCh37.p13 chr3: 84,714,110-84,714,167 LINC00971
    nsv5446643copy number variation1nstd206human GRCh38 chr3: 84,817,411-84,822,760 , GRCh37.p13 chr3: 84,866,562-84,871,911 LINC00971
    nsv5435134copy number variation1nstd206human GRCh38 chr3: 84,684,000-84,700,000 , GRCh37.p13 chr3: 84,733,151-84,749,151 TMEM183AP5, LINC00971
    nsv5434969copy number variation1nstd206human GRCh38 chr3: 84,650,355-84,653,734 , GRCh37.p13 chr3: 84,699,506-84,702,885 LINC00971
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