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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5902627copy number variation1nstd209human GRCh38 chr3: 101,847,594-101,847,821 , GRCh37.p13 chr3: 101,566,438-101,566,665 NFKBIZ
    nsv5716077mobile element insertion1nstd211human GRCh38 chr3: 101,846,172-101,846,172 , GRCh37.p13 chr3: 101,565,016-101,565,016 NFKBIZ
    nsv5313202copy number variation1nstd204human GRCh38.p13 chr3: 101,838,038-101,844,683 , GRCh37.p13 chr3: 101,556,882-101,563,527 NFKBIZ
    nsv5302429copy number variation1nstd204human GRCh38.p13 chr3: 101,840,825-101,844,682 , GRCh37.p13 chr3: 101,559,669-101,563,526 NFKBIZ
    nsv5237544copy number variation1nstd204human GRCh38.p13 chr3: 101,838,930-101,844,594 , GRCh37.p13 chr3: 101,557,774-101,563,438 NFKBIZ
    nsv5036857inversion1nstd200human GRCh38 chr3: 97,392,267-146,717,859 , GRCh37.p13 chr3: 97,111,111-146,435,646 , FBRSL1P1, 801 more genes
    nsv5034224inversion1nstd200human GRCh38 chr3: 94,859,289-102,665,887 , GRCh37.p13 chr3: 94,578,133-102,384,731 , LOC105374005, 114 more genes
    nsv4919211copy number variation1nstd200human GRCh38 chr3: 101,847,597-101,847,822 , GRCh37.p13 chr3: 101,566,441-101,566,666 NFKBIZ
    nsv4919210copy number variation1nstd200human GRCh38 chr3: 101,843,182-101,845,003 , GRCh37.p13 chr3: 101,562,026-101,563,847 NFKBIZ
    nsv4797718copy number variation1nstd200human GRCh37 chr3: 101,562,026-101,563,847 , GRCh38.p12 chr3: 101,843,182-101,845,003 NFKBIZ
    nsv4728581copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 95,563,096-102,371,126 , GRCh38.p12 chr3: 95,844,252-102,652,282 COL8A1, CPOX, 107 more genes
    nsv4586976copy number variation1nstd183human GRCh37 chr3: 101,578,340-101,579,550 , GRCh38.p12 chr3: 101,859,496-101,860,706 NFKBIZ
    nsv4584475copy number variation1nstd183human GRCh37 chr3: 101,548,650-101,573,886 , GRCh38.p12 chr3: 101,829,806-101,855,042 NFKBIZ
    nsv4520641copy number variation1nstd166human GRCh37.p13 chr3: 101,305,028-101,858,244 , GRCh38.p12 chr3: 101,586,184-102,139,400 , NXPE3, 11 more genes
    nsv4323076inversion1nstd166human GRCh37.p13 chr3: 100,669,301-101,957,545 , GRCh38.p12 chr3: 100,950,457-102,238,701 , CEP97, 23 more genes
    nsv4089626copy number variation1nstd166human GRCh37.p13 chr3: 101,566,441-101,566,666 , GRCh38.p12 chr3: 101,847,597-101,847,822 NFKBIZ
    nsv4088324copy number variation1nstd166human GRCh37.p13 chr3: 101,562,026-101,563,847 , GRCh38.p12 chr3: 101,843,182-101,845,003 NFKBIZ
    nsv3922717copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,002,154-146,895,858 , GRCh38 chr3: 93,800,620-145,695,381 , GRCh37 chr3: 93,519,464-145,413,168 OR7E53P, HSPA8P9, 794 more genes
    nsv3919242copy number variation1nstd102humanLikely benign GRCh38 chr3: 101,596,165-102,374,145 , NCBI36 chr3: 102,797,699-103,575,679 , GRCh37 chr3: 101,315,009-102,092,989 NFKBIZ, CEP97, 11 more genes
    nsv3918661copy number variation1nstd102humanPathogenic NCBI36 chr3: 95,088,205-124,418,220 , GRCh37 chr3: 93,605,515-122,935,530 , GRCh38 chr3: 93,886,671-123,216,683 MTCO2P29, GAP43, 401 more genes
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