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Items: 1 to 20 of 182

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5978257insertion1nstd209human GRCh38 chr16: 55,687,190-55,687,190 , GRCh37.p13 chr16: 55,721,102-55,721,102 SLC6A2
    nsv5660369insertion1nstd207human GRCh38 chr16: 55,687,190-55,687,190 , GRCh37.p13 chr16: 55,721,102-55,721,102 SLC6A2
    nsv5549716insertion1nstd206human GRCh38 chr16: 55,687,190-55,687,190 , GRCh37.p13 chr16: 55,721,102-55,721,102 SLC6A2
    nsv5531002copy number variation1nstd206human GRCh38 chr16: 55,694,682-55,763,000 , GRCh37.p13 chr16: 55,728,594-55,796,912 SLC6A2, CES1P1, 2 more genes
    nsv5523861copy number variation1nstd206human GRCh38 chr16: 55,704,485-55,704,573 , GRCh37.p13 chr16: 55,738,397-55,738,485 SLC6A2
    nsv5143905mobile element insertion1nstd203human GRCh38 chr16: 55,658,980-55,658,995 , GRCh37.p13 chr16: 55,692,892-55,692,907 SLC6A2
    nsv5008339copy number variation1nstd200human GRCh38 chr16: 55,704,485-55,704,581 , GRCh37.p13 chr16: 55,738,397-55,738,493 SLC6A2
    nsv4761046insertion1nstd199human GRCh37 chr16: 55,721,101-55,721,101 , GRCh38.p12 chr16: 55,687,189-55,687,189 SLC6A2
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4725208insertion3nstd186human GRCh37 chr16: 55,721,102-55,721,102 , GRCh38.p12 chr16: 55,687,190-55,687,190 SLC6A2
    nsv4685026insertion1nstd194human GRCh37 chr16: 55,721,102-55,721,102 , GRCh38.p12 chr16: 55,687,190-55,687,190 SLC6A2
    nsv4456077copy number variation1nstd102humanUncertain significance GRCh37 chr16: 53,455,650-64,006,604 , GRCh38.p12 chr16: 53,421,738-63,972,700 MT1DP, RPL23AP91, 167 more genes
    nsv4438048insertion1nstd175human GRCh37 chr16: 55,721,102-55,721,102 , GRCh38.p12 chr16: 55,687,190-55,687,190 SLC6A2
    nsv4428747copy number variation1nstd174human GRCh37 chr16: 55,729,562-55,784,484 , GRCh38.p12 chr16: 55,695,650-55,750,572 CES1P2, SLC6A2, 1 more genes
    nsv4365843copy number variation1nstd173human GRCh37 chr16: 46,464,489-55,795,214 , GRCh38.p12 chr16: 46,430,577-55,761,302 , LOC100526838, 158 more genes
    nsv4365186copy number variation1nstd173human GRCh37 chr16: 46,503,205-57,376,253 , GRCh38.p12 chr16: 46,469,293-57,342,341 , TOX3, 210 more genes
    nsv4329126insertion1nstd166human GRCh37.p13 chr16: 55,721,102-55,721,102 , GRCh38.p12 chr16: 55,687,190-55,687,190 SLC6A2
    nsv4240267copy number variation1nstd166human GRCh37.p13 chr16: 55,696,636-55,696,854 , GRCh38.p12 chr16: 55,662,724-55,662,942 SLC6A2
    nsv3964140copy number variation1nstd168human GRCh38 chr16: 55,706,293-55,784,144 , GRCh37.p13 chr16: 55,740,205-55,818,056 CES1P1, CES1P2, 2 more genes
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