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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5891827copy number variation1nstd209human GRCh38 chr3: 45,726,859-45,727,183 , GRCh37.p13 chr3: 45,768,351-45,768,675 SACM1L
    nsv5684470mobile element insertion2nstd211human GRCh38 chr3: 45,714,193-45,714,193 , GRCh37.p13 chr3: 45,755,685-45,755,685 SACM1L
    nsv5568319copy number variation1nstd207human GRCh38 chr3: 45,726,859-45,727,183 , GRCh37.p13 chr3: 45,768,351-45,768,675 SACM1L
    nsv5453277copy number variation1nstd206human GRCh38 chr3: 45,730,568-45,730,633 , GRCh37.p13 chr3: 45,772,060-45,772,125 SACM1L
    nsv5446499copy number variation1nstd206human GRCh38 chr3: 45,726,869-45,727,184 , GRCh37.p13 chr3: 45,768,361-45,768,676 SACM1L
    nsv5436577copy number variation1nstd206human GRCh38 chr3: 45,711,742-45,712,849 , GRCh37.p13 chr3: 45,753,234-45,754,341 SACM1L
    nsv5405587mobile element insertion1nstd206human GRCh38 chr3: 45,714,193-45,714,210 , GRCh37.p13 chr3: 45,755,685-45,755,702 SACM1L
    nsv5383905mobile element deletion2nstd186human GRCh37 chr3: 45,768,361-45,768,676 , GRCh38.p12 chr3: 45,726,869-45,727,184 SACM1L
    nsv5218408mobile element deletion1nstd204human GRCh38.p13 chr3: 45,726,869-45,727,184 , GRCh37.p13 chr3: 45,768,361-45,768,676 SACM1L
    nsv5202963copy number variation1nstd204human GRCh38.p13 chr3: 45,726,901-45,727,200 , GRCh37.p13 chr3: 45,768,393-45,768,692 SACM1L
    nsv5175220mobile element insertion1nstd203human GRCh38 chr3: 45,717,979-45,717,997 , GRCh37.p13 chr3: 45,759,471-45,759,489 SACM1L
    nsv5078881mobile element insertion1nstd203human GRCh38 chr3: 45,716,321-45,716,339 , GRCh37.p13 chr3: 45,757,813-45,757,831 SACM1L
    nsv5075164mobile element insertion1nstd203human GRCh38 chr3: 45,707,887-45,707,900 , GRCh37.p13 chr3: 45,749,379-45,749,392 SACM1L
    nsv5061870mobile element insertion1nstd203human GRCh38 chr3: 45,714,193-45,714,210 , GRCh37.p13 chr3: 45,755,685-45,755,702 SACM1L
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4911096copy number variation1nstd200human GRCh38 chr3: 45,745,752-45,748,314 , GRCh37.p13 chr3: 45,787,244-45,789,806 SACM1L
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4887120mobile element deletion1nstd200human GRCh38 chr3: 45,726,869-45,727,184 , GRCh37.p13 chr3: 45,768,361-45,768,676 SACM1L
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
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