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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137722copy number variation1nstd102humanBenign GRCh38 chr16: 579,448-579,519 , GRCh37 chr16: 629,448-629,519 PIGQ
    nsv6137721copy number variation1nstd102humanBenign GRCh37 chr16: 629,428-629,499 , GRCh38 chr16: 579,428-579,499 PIGQ
    nsv6112797copy number variation1nstd102humanPathogenic GRCh37 chr16: 84,485-5,251,013 , GRCh38.p12 chr16: 34,485-5,201,012 ANTKMT, HBA1, 307 more genes
    nsv5657958insertion1nstd207human GRCh38 chr16: 571,109-571,109 , GRCh37.p13 chr16: 621,109-621,109 PIGQ
    nsv5601619copy number variation1nstd207human GRCh38 chr16: 579,427-579,594 , GRCh37.p13 chr16: 629,427-629,594 PIGQ
    nsv5593332copy number variation1nstd207human GRCh38 chr16: 571,143-571,433 , GRCh37.p13 chr16: 621,143-621,433 PIGQ
    nsv5590298copy number variation1nstd207human GRCh38 chr16: 579,427-579,498 , GRCh37.p13 chr16: 629,427-629,498 PIGQ
    nsv5380998copy number variation2nstd102humanUncertain significance GRCh37 chr16: 624,055-2,153,916 , GRCh38.p12 chr16: 574,055-2,103,915 NDUFB10, BAIAP3, 102 more genes
    nsv5309848copy number variation1nstd204human GRCh38.p13 chr16: 572,271-572,594 , GRCh37.p13 chr16: 622,271-622,594 PIGQ
    nsv5278593copy number variation1nstd204human GRCh38.p13 chr16: 495,101-1,599,500 , GRCh37.p13 chr16: 545,101-1,649,501 , MIR662, 73 more genes
    nsv5265522copy number variation1nstd204human GRCh38.p13 chr16: 53,201-2,576,200 , GRCh37.p13 chr16: 103,201-2,626,201 , RHBDL1, 175 more genes
    nsv5263615copy number variation1nstd204human GRCh38.p13 chr16: 504,601-857,400 , GRCh37.p13 chr16: 554,601-907,400 , LINC00235, 36 more genes
    nsv5009321copy number variation1nstd200human GRCh38 chr16: 584,489-589,099 , GRCh37.p13 chr16: 634,489-639,099 PIGQ, RAB40C
    nsv5002874copy number variation1nstd200human GRCh38 chr16: 580,923-581,497 , GRCh37.p13 chr16: 630,923-631,497 PIGQ
    nsv4866304copy number variation1nstd200human GRCh37 chr16: 630,922-631,497 , GRCh38.p12 chr16: 580,922-581,497 PIGQ
    nsv4866303copy number variation1nstd200human GRCh37 chr16: 622,280-622,586 , GRCh38.p12 chr16: 572,280-572,586 PIGQ
    nsv4749389copy number variation1nstd199human GRCh37 chr16: 629,431-629,550 , GRCh38.p12 chr16: 579,431-579,550 PIGQ
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
    nsv4683390copy number variation1nstd102humanPathogenic GRCh37 chr16: 624,055-2,148,005 , GRCh38.p12 chr16: 574,055-2,098,004 MRPS34, HAGHL, 102 more genes
    nsv4682518copy number variation1nstd102humanUncertain significance GRCh37 chr16: 624,055-2,550,979 , GRCh38.p12 chr16: 574,055-2,500,978 C1QTNF8, NHERF2, 133 more genes
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