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Items: 1 to 20 of 175

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112738copy number variation1nstd102humanPathogenic GRCh37 chr6: 149,619-3,951,208 , GRCh38.p12 chr6: 149,619-3,950,974 LINC01600, TUBB2BP1, 66 more genes
    nsv5957529insertion1nstd209human GRCh38 chr6: 2,893,191-2,893,191 , GRCh37.p13 chr6: 2,893,425-2,893,425 SERPINB9, SERPINB9-AS1
    nsv5634208insertion3nstd207human GRCh38 chr6: 2,893,191-2,893,191 , GRCh37.p13 chr6: 2,893,425-2,893,425 SERPINB9, SERPINB9-AS1
    nsv5582905copy number variation1nstd207human GRCh38 chr6: 2,888,823-2,889,236 , GRCh37.p13 chr6: 2,889,057-2,889,470 SERPINB9, SERPINB9-AS1
    nsv5548660insertion1nstd206human GRCh38 chr6: 2,893,203-2,893,203 , GRCh37.p13 chr6: 2,893,437-2,893,437 SERPINB9, SERPINB9-AS1
    nsv5465083copy number variation1nstd206human GRCh38 chr6: 2,888,823-2,889,243 , GRCh37.p13 chr6: 2,889,057-2,889,477 SERPINB9, SERPINB9-AS1
    nsv5381385copy number variation2nstd102humanUncertain significance GRCh37 chr6: 2,833,842-3,227,777 , GRCh38.p12 chr6: 2,833,608-3,227,543 SERPINB9-AS1, RIPK1, 20 more genes
    nsv5227852copy number variation1nstd204human GRCh38.p13 chr6: 2,883,201-2,970,200 , GRCh37.p13 chr6: 2,883,435-2,970,434 , SERPINB9-AS1, 2 more genes
    nsv5183261mobile element insertion1nstd203human GRCh38 chr6: 2,886,852-2,886,867 , GRCh37.p13 chr6: 2,887,086-2,887,101 SERPINB9, SERPINB9-AS1
    nsv4809464copy number variation1nstd200human GRCh37 chr6: 2,889,057-2,889,477 , GRCh38.p12 chr6: 2,888,823-2,889,243 SERPINB9-AS1, SERPINB9
    nsv4767548insertion1nstd199human GRCh37 chr6: 2,893,434-2,893,434 , GRCh38.p12 chr6: 2,893,200-2,893,200 SERPINB9, SERPINB9-AS1
    nsv4729315copy number variation1nstd102humanPathogenic GRCh37 chr6: 302,183-3,290,583 , GRCh38.p12 chr6: 302,183-3,290,349 RIPK1, MARK2P18, 53 more genes
    nsv4592248copy number variation1nstd183human GRCh37 chr6: 2,889,495-2,894,608 , GRCh38.p12 chr6: 2,889,261-2,894,374 SERPINB9, SERPINB9-AS1
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4128657copy number variation1nstd166human GRCh37.p13 chr6: 2,889,057-2,889,477 , GRCh38.p12 chr6: 2,888,823-2,889,243 SERPINB9, SERPINB9-AS1
    nsv4116994copy number variation1nstd166human GRCh37.p13 chr6: 2,867,240-2,905,607 , GRCh38.p12 chr6: 2,867,006-2,905,373 SERPINB9P1, SERPINB9, 1 more genes
    nsv3967721insertion1nstd168human GRCh38 chr6: 2,902,885-2,962,577 , GRCh37.p13 chr6: 2,903,119-2,962,811 , SERPINB6, 1 more genes
    nsv3931002insertion1nstd167human GRCh37 chr6: 2,893,425-2,893,425 , GRCh38.p12 chr6: 2,893,191-2,893,191 SERPINB9, SERPINB9-AS1
    nsv3923249copy number variation1nstd102humanPathogenic NCBI36 chr6: 110,675-8,981,266 , GRCh38 chr6: 165,675-9,036,034 , GRCh37 chr6: 165,675-9,036,267 LOC100506207, LOC105374889, 148 more genes
    nsv3923206copy number variation1nstd102humanPathogenic NCBI36 chr6: 108,083-3,404,840 , GRCh38 chr6: 163,083-3,459,607 , GRCh37 chr6: 163,083-3,459,841 LOC105374883, MIR4645, 58 more genes
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