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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137672copy number variation1nstd102humannot provided GRCh38 chr2: 124,348,648-129,410,245 , GRCh37.p13 chr2: 125,106,225-130,167,818 LOC105373603, MYO7B, 59 more genes
    nsv5955241insertion1nstd209human GRCh38 chr2: 127,192,754-127,192,754 , GRCh37.p13 chr2: 127,950,330-127,950,330 CYP27C1
    nsv5687403mobile element insertion1nstd211human GRCh38 chr2: 127,204,555-127,204,555 , GRCh37.p13 chr2: 127,962,131-127,962,131 CYP27C1
    nsv5680916mobile element insertion2nstd211human GRCh38 chr2: 127,188,684-127,188,684 , GRCh37.p13 chr2: 127,946,260-127,946,260 CYP27C1
    nsv5679440mobile element insertion1nstd211human GRCh38 chr2: 127,204,440-127,204,440 , GRCh37.p13 chr2: 127,962,016-127,962,016 CYP27C1
    nsv5609538insertion1nstd207human GRCh38 chr2: 127,188,668-127,188,668 , GRCh37.p13 chr2: 127,946,244-127,946,244 CYP27C1
    nsv5605370insertion1nstd207human GRCh38 chr2: 127,192,756-127,192,756 , GRCh37.p13 chr2: 127,950,332-127,950,332 CYP27C1
    nsv5578567copy number variation1nstd207human GRCh38 chr2: 127,204,468-127,204,530 , GRCh37.p13 chr2: 127,962,044-127,962,106 CYP27C1
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5550925insertion1nstd206human GRCh38 chr2: 127,192,753-127,192,753 , GRCh37.p13 chr2: 127,950,329-127,950,329 CYP27C1
    nsv5446549copy number variation1nstd206human GRCh38 chr2: 127,170,686-127,212,336 , GRCh37.p13 chr2: 127,928,262-127,969,912 NIFKP9, CYP27C1
    nsv5395126mobile element insertion1nstd206human GRCh38 chr2: 127,188,684-127,188,735 , GRCh37.p13 chr2: 127,946,260-127,946,311 CYP27C1
    nsv5217734copy number variation1nstd204human GRCh38.p13 chr2: 127,210,550-127,213,018 , GRCh37.p13 chr2: 127,968,126-127,970,594 CYP27C1
    nsv5217697copy number variation1nstd204human GRCh38.p13 chr2: 127,212,865-127,214,957 , GRCh37.p13 chr2: 127,970,441-127,972,533 CYP27C1
    nsv5078889mobile element insertion1nstd203human GRCh38 chr2: 127,188,684-127,188,684 , GRCh37.p13 chr2: 127,946,260-127,946,260 CYP27C1
    nsv5071469mobile element insertion1nstd203human GRCh38 chr2: 127,188,672-127,188,684 , GRCh37.p13 chr2: 127,946,248-127,946,260 CYP27C1
    nsv5071300mobile element insertion1nstd203human GRCh38 chr2: 127,188,668-127,188,678 , GRCh37.p13 chr2: 127,946,244-127,946,254 CYP27C1
    nsv5068352mobile element insertion1nstd203human GRCh38 chr2: 127,188,675-127,188,684 , GRCh37.p13 chr2: 127,946,251-127,946,260 CYP27C1
    nsv5060828mobile element insertion1nstd203human GRCh38 chr2: 127,188,673-127,188,684 , GRCh37.p13 chr2: 127,946,249-127,946,260 CYP27C1
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