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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5959416insertion1nstd209human GRCh38 chr6: 70,729,453-70,729,453 , GRCh37.p13 chr6: 71,439,156-71,439,156 SMAP1
    nsv5694184mobile element insertion1nstd211human GRCh38 chr6: 70,789,606-70,789,606 , GRCh37.p13 chr6: 71,499,309-71,499,309 SMAP1
    nsv5685615mobile element insertion1nstd211human GRCh38 chr6: 70,783,330-70,783,330 , GRCh37.p13 chr6: 71,493,033-71,493,033 SMAP1
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5553685insertion1nstd206human GRCh38 chr6: 70,726,091-70,726,094 , GRCh37.p13 chr6: 71,435,794-71,435,797 SMAP1
    nsv5461766copy number variation1nstd206human GRCh38 chr6: 70,783,003-70,783,067 , GRCh37.p13 chr6: 71,492,706-71,492,770 SMAP1
    nsv5455901copy number variation1nstd206human GRCh38 chr6: 70,658,797-70,667,526 , GRCh37.p13 chr6: 71,368,500-71,377,229 SMAP1, SLC25A6P6
    nsv5406748mobile element insertion1nstd206human GRCh38 chr6: 70,767,580-70,767,631 , GRCh37.p13 chr6: 71,477,283-71,477,334 SMAP1
    nsv5404154mobile element insertion1nstd206human GRCh38 chr6: 70,783,330-70,783,348 , GRCh37.p13 chr6: 71,493,033-71,493,051 SMAP1
    nsv5363172translocation1nstd200human GRCh38 chr6: 70,800,947-70,800,947 , GRCh38 chr6: 70,800,891-70,800,891 , GRCh37.p13 chr6: 71,510,650-71,510,650 , GRCh37.p13 chr6: 71,510,594-71,510,594 SMAP1
    nsv5333399translocation1nstd200human GRCh37 chr6: 71,376,777-71,376,777 , GRCh37 chr11: 6,389,831-6,389,831 , GRCh38.p12 chr11: 6,368,601-6,368,601 , GRCh38.p12 chr6: 70,667,074-70,667,074 SMAP1
    nsv5312312copy number variation1nstd204human GRCh38.p13 chr6: 70,417,080-71,173,678 , GRCh37.p13 chr6: 71,126,783-71,883,381 LOC100419975, FAM135A, 9 more genes
    nsv5235177copy number variation1nstd204human GRCh38.p13 chr6: 70,815,645-70,846,268 , GRCh37.p13 chr6: 71,525,348-71,555,971 SMAP1
    nsv5234851copy number variation1nstd204human GRCh38.p13 chr6: 70,824,354-70,827,553 , GRCh37.p13 chr6: 71,534,057-71,537,256 SMAP1
    nsv5233466copy number variation1nstd204human GRCh38.p13 chr6: 70,766,401-70,767,400 , GRCh37.p13 chr6: 71,476,104-71,477,103 SMAP1
    nsv5232783copy number variation1nstd204human GRCh38.p13 chr6: 70,417,301-71,173,300 , GRCh37.p13 chr6: 71,127,004-71,883,003 LOC100419975, LYPLA1P3, 9 more genes
    nsv5231742copy number variation1nstd204human GRCh38.p13 chr6: 70,610,500-70,682,790 , GRCh37.p13 chr6: 71,320,203-71,392,493 SMAP1, SLC25A6P6
    nsv5221902copy number variation1nstd204human GRCh38.p13 chr6: 70,766,681-70,815,494 , GRCh37.p13 chr6: 71,476,384-71,525,197 SMAP1
    nsv5176457mobile element insertion1nstd203human GRCh38 chr6: 70,823,184-70,823,196 , GRCh37.p13 chr6: 71,532,887-71,532,899 SMAP1
    nsv5165323mobile element insertion1nstd203human GRCh38 chr6: 70,712,764-70,712,811 , GRCh37.p13 chr6: 71,422,467-71,422,514 SMAP1
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