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Items: 1 to 20 of 208

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5698007mobile element insertion2nstd211human GRCh38 chr16: 3,587,690-3,587,690 , GRCh37.p13 chr16: 3,637,691-3,637,691 SLX4
    nsv5674298delins1nstd102humanPathogenic GRCh37 chr16: 3,640,492-3,645,381 , GRCh38 chr16: 3,590,491-3,595,380 SLX4
    nsv5672997copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,658,425-3,658,971 , GRCh38.p12 chr16: 3,608,424-3,608,970 SLX4
    nsv5657607insertion1nstd207human GRCh38 chr16: 3,587,674-3,587,674 , GRCh37.p13 chr16: 3,637,675-3,637,675 SLX4
    nsv5653605insertion1nstd207human GRCh38 chr16: 3,584,378-3,584,378 , GRCh37.p13 chr16: 3,634,379-3,634,379 SLX4
    nsv5515798copy number variation1nstd206human GRCh38 chr16: 3,584,097-3,585,887 , GRCh37.p13 chr16: 3,634,098-3,635,888 SLX4
    nsv5424863mobile element insertion1nstd206human GRCh38 chr16: 3,587,690-3,587,720 , GRCh37.p13 chr16: 3,637,691-3,637,721 SLX4
    nsv5349428translocation1nstd200human GRCh38 chr16: 3,611,636-3,611,636 , GRCh38 chr16: 3,611,545-3,611,545 , GRCh37.p13 chr16: 3,661,546-3,661,546 , GRCh37.p13 chr16: 3,661,637-3,661,637 DNASE1, SLX4
    nsv5158959mobile element insertion1nstd203human GRCh38 chr16: 3,587,674-3,587,689 , GRCh37.p13 chr16: 3,637,675-3,637,690 SLX4
    nsv5145495mobile element insertion1nstd203human GRCh38 chr16: 3,587,681-3,587,690 , GRCh37.p13 chr16: 3,637,682-3,637,691 SLX4
    nsv5141055mobile element insertion1nstd203human GRCh38 chr16: 3,587,680-3,587,690 , GRCh37.p13 chr16: 3,637,681-3,637,691 SLX4
    nsv5009387copy number variation1nstd200human GRCh38 chr16: 3,584,296-3,585,643 , GRCh37.p13 chr16: 3,634,297-3,635,644 SLX4
    nsv4729901copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,959,279-30,190,593 , GRCh38.p12 chr16: 2,909,278-30,179,272 NPIPB9, TMEM219, 597 more genes
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
    nsv4729144copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,598,059-3,738,078 , GRCh38.p12 chr16: 3,548,059-3,688,077 SLX4, DNASE1, 4 more genes
    nsv4681284copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,656,465-3,658,975 , GRCh38.p12 chr16: 3,606,464-3,608,974 SLX4
    nsv4675826copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,651,354-4,614,965 , GRCh38.p12 chr16: 2,601,353-4,564,964 MEFV, TRR-CCT5-1, 111 more genes
    nsv4629429copy number variation2nstd183human GRCh37 chr16: 3,661,776-3,661,829 , GRCh38.p12 chr16: 3,611,775-3,611,828 SLX4, DNASE1
    nsv4622946copy number variation1nstd183human GRCh37 chr16: 3,627,027-3,709,523 , GRCh38.p12 chr16: 3,577,026-3,659,522 SLX4, LOC105371060, 3 more genes
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