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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977795inversion1nstd209human GRCh38 chr12: 75,286,460-75,296,027 , GRCh37.p13 chr12: 75,680,240-75,689,807 CAPS2, CAPS2-AS1
    nsv5974022insertion1nstd209human GRCh38 chr12: 75,288,349-75,288,349 , GRCh37.p13 chr12: 75,682,129-75,682,129 CAPS2, CAPS2-AS1
    nsv5860156copy number variation2nstd209human GRCh38 chr12: 75,296,019-75,298,076 , GRCh37.p13 chr12: 75,689,799-75,691,856 CAPS2, CAPS2-AS1
    nsv5851842copy number variation1nstd209human GRCh38 chr12: 75,295,457-75,299,376 , GRCh37.p13 chr12: 75,689,237-75,693,156 CAPS2, CAPS2-AS1
    nsv5700561mobile element insertion2nstd211human GRCh38 chr12: 75,288,360-75,288,360 , GRCh37.p13 chr12: 75,682,140-75,682,140 CAPS2-AS1, CAPS2
    nsv5653927insertion1nstd207human GRCh38 chr12: 75,288,349-75,288,349 , GRCh37.p13 chr12: 75,682,129-75,682,129 CAPS2-AS1, CAPS2
    nsv5541079insertion1nstd206human GRCh38 chr12: 75,292,697-75,292,748 , GRCh37.p13 chr12: 75,686,477-75,686,528 CAPS2, CAPS2-AS1
    nsv5512296copy number variation1nstd206human GRCh38 chr12: 75,275,980-75,276,139 , GRCh37.p13 chr12: 75,669,760-75,669,919 CAPS2-AS1, CAPS2
    nsv5418675mobile element insertion1nstd206human GRCh38 chr12: 75,288,360-75,288,411 , GRCh37.p13 chr12: 75,682,140-75,682,191 CAPS2, CAPS2-AS1
    nsv5276688copy number variation1nstd204human GRCh38.p13 chr12: 75,275,601-75,282,000 , GRCh37.p13 chr12: 75,669,381-75,675,780 CAPS2-AS1, CAPS2
    nsv5262601copy number variation1nstd204human GRCh38.p13 chr12: 75,276,201-75,286,800 , GRCh37.p13 chr12: 75,669,981-75,680,580 CAPS2, CAPS2-AS1
    nsv5138922mobile element insertion1nstd203human GRCh38 chr12: 75,288,353-75,288,360 , GRCh37.p13 chr12: 75,682,133-75,682,140 CAPS2-AS1, CAPS2
    nsv5132879mobile element insertion1nstd203human GRCh38 chr12: 75,278,400-75,278,413 , GRCh37.p13 chr12: 75,672,180-75,672,193 CAPS2-AS1, CAPS2
    nsv5131443mobile element insertion1nstd203human GRCh38 chr12: 75,261,496-75,261,510 , GRCh37.p13 chr12: 75,655,276-75,655,290 CAPS2-AS1
    nsv5128917mobile element insertion1nstd203human GRCh38 chr12: 75,288,349-75,288,360 , GRCh37.p13 chr12: 75,682,129-75,682,140 CAPS2-AS1, CAPS2
    nsv5125629mobile element insertion1nstd203human GRCh38 chr12: 75,288,352-75,288,360 , GRCh37.p13 chr12: 75,682,132-75,682,140 CAPS2-AS1, CAPS2
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv5032581inversion1nstd200human GRCh38 chr12: 67,763,754-90,678,993 , GRCh37.p13 chr12: 68,157,534-91,072,770 , LOC105369886, 255 more genes
    nsv5006102copy number variation1nstd200human GRCh38 chr12: 75,286,384-75,289,647 , GRCh37.p13 chr12: 75,680,164-75,683,427 CAPS2, CAPS2-AS1
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