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Items: 1 to 20 of 571

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5905914copy number variation1nstd209human GRCh38 chr2: 241,765,479-241,767,392 , GRCh37.p13 chr2: 242,704,894-242,706,807 D2HGDH
    nsv5903610copy number variation1nstd209human GRCh38 chr2: 241,755,607-241,755,684 , GRCh37.p13 chr2: 242,695,022-242,695,099 D2HGDH
    nsv5900619copy number variation1nstd209human GRCh38 chr2: 241,742,860-241,743,139 , GRCh37.p13 chr2: 242,682,275-242,682,554 D2HGDH
    nsv5898268copy number variation1nstd209human GRCh38 chr2: 241,751,996-241,752,072 , GRCh37.p13 chr2: 242,691,411-242,691,487 D2HGDH
    nsv5897859copy number variation1nstd209human GRCh38 chr2: 241,749,737-241,749,866 , GRCh37.p13 chr2: 242,689,152-242,689,281 D2HGDH
    nsv5894144copy number variation1nstd209human GRCh38 chr2: 241,730,492-241,735,968 , GRCh37.p13 chr2: 242,669,907-242,675,383 D2HGDH
    nsv5888187copy number variation1nstd209human GRCh38 chr2: 241,765,455-241,767,248 , GRCh37.p13 chr2: 242,704,870-242,706,663 D2HGDH
    nsv5623059insertion1nstd207human GRCh38 chr2: 241,751,964-241,751,964 , GRCh37.p13 chr2: 242,691,379-242,691,379 D2HGDH
    nsv5621091insertion1nstd207human GRCh38 chr2: 241,743,140-241,743,140 , GRCh37.p13 chr2: 242,682,555-242,682,555 D2HGDH
    nsv5609729insertion1nstd207human GRCh38 chr2: 241,760,510-241,760,510 , GRCh37.p13 chr2: 242,699,925-242,699,925 D2HGDH
    nsv5609094insertion1nstd207human GRCh38 chr2: 241,755,607-241,755,607 , GRCh37.p13 chr2: 242,695,022-242,695,022 D2HGDH
    nsv5580168copy number variation1nstd207human GRCh38 chr2: 241,765,436-241,765,485 , GRCh37.p13 chr2: 242,704,851-242,704,900 D2HGDH
    nsv5573316copy number variation1nstd207human GRCh38 chr2: 241,765,305-241,766,704 , GRCh37.p13 chr2: 242,704,720-242,706,119 D2HGDH
    nsv5571349copy number variation1nstd207human GRCh38 chr2: 241,760,089-241,760,174 , GRCh37.p13 chr2: 242,699,504-242,699,589 D2HGDH
    nsv5569819copy number variation1nstd207human GRCh38 chr2: 241,766,055-241,766,204 , GRCh37.p13 chr2: 242,705,470-242,705,619 D2HGDH
    nsv5565739copy number variation1nstd207human GRCh38 chr2: 241,757,383-241,757,459 , GRCh37.p13 chr2: 242,696,798-242,696,874 D2HGDH
    nsv5565393copy number variation1nstd207human GRCh38 chr2: 241,741,527-241,741,628 , GRCh37.p13 chr2: 242,680,942-242,681,043 D2HGDH
    nsv5564614copy number variation1nstd207human GRCh38 chr2: 241,742,918-241,742,997 , GRCh37.p13 chr2: 242,682,333-242,682,412 D2HGDH
    nsv5544918insertion1nstd206human GRCh38 chr2: 241,755,562-241,755,612 , GRCh37.p13 chr2: 242,694,977-242,695,027 D2HGDH
    nsv5445538copy number variation1nstd206human GRCh38 chr2: 241,733,049-241,747,519 , GRCh37.p13 chr2: 242,672,464-242,686,934 D2HGDH
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