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Items: 1 to 20 of 195

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5928160copy number variation1nstd209human GRCh38 chr16: 28,496,037-28,496,114 , GRCh37.p13 chr16: 28,507,358-28,507,435 APOBR
    nsv5728917mobile element insertion2nstd211human GRCh38 chr16: 28,493,775-28,493,775 , GRCh37.p13 chr16: 28,505,096-28,505,096 APOBR
    nsv5673078copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,488,827-28,950,294 , GRCh38.p12 chr16: 28,477,506-28,938,973 SH2B1, NUPR1, 21 more genes
    nsv5669869inversion1nstd207human GRCh38 chr16: 28,471,894-28,637,650 , GRCh37.p13 chr16: 28,483,215-28,648,971 CLN3, SULT1A2, 7 more genes
    nsv5563648mobile element insertion1nstd206human GRCh38 chr16: 28,493,775-28,493,826 , GRCh37.p13 chr16: 28,505,096-28,505,147 APOBR
    nsv5195188mobile element insertion1nstd203human GRCh38 chr16: 28,493,756-28,493,775 , GRCh37.p13 chr16: 28,505,077-28,505,096 APOBR
    nsv4769395copy number variation1nstd102humanUncertain significance GRCh37 chr16: 28,483,631-29,332,591 , GRCh38.p12 chr16: 28,472,310-29,321,270 MIR4517, SULT1A1, 33 more genes
    nsv4730105inversion12nstd198human GRCh38 chr16: 28,339,079-28,822,601 , GRCh37.p13 chr16: 28,350,400-28,833,922 , CLN3, 22 more genes
    nsv4729918copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,488,319-30,178,406 , GRCh38.p12 chr16: 28,476,998-30,167,085 SEZ6L2, C16orf92, 81 more genes
    nsv4729912copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,336,673-29,358,712 , GRCh38.p12 chr16: 28,325,352-29,347,391 ATP2A1-AS1, NPIPB8, 38 more genes
    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
    nsv4685985copy number variation1nstd102humanPathogenic GRCh37 chr16: 5,805,001-34,230,001 , GRCh38.p12 chr16: 5,755,000-34,995,630 LOC105371069, PKD1P6-NPIPP1, 654 more genes
    nsv4685761copy number variation1nstd102humannot provided GRCh37 chr16: 21,312,200-29,646,379 , GRCh38.p12 chr16: 21,300,879-29,635,058 NUPR1, TNRC6A, 176 more genes
    nsv4675970copy number variation1nstd102humanPathogenic GRCh37 chr16: 21,576,802-29,351,826 , GRCh38.p12 chr16: 21,565,481-29,340,505 NSMCE1, LOC105371149, 152 more genes
    nsv4674913copy number variation1nstd102humanPathogenic GRCh37 chr16: 28,466,730-30,178,406 , GRCh38.p12 chr16: 28,455,409-30,167,085 ATP2A1, IL27, 82 more genes
    nsv4658000inversion1nstd185human GRCh37.p13 chr16: 28,483,213-28,654,502 , GRCh38.p13 chr16: 28,471,892-28,643,181 CLN3, SULT1A2, 7 more genes
    nsv4576252mobile element insertion1nstd166human GRCh37.p13 chr16: 28,505,077-28,505,077 , GRCh38.p12 chr16: 28,493,756-28,493,756 APOBR
    nsv4574606mobile element insertion1nstd166human GRCh37.p13 chr16: 28,505,096-28,505,096 , GRCh38.p12 chr16: 28,493,775-28,493,775 APOBR
    nsv4531429copy number variation1nstd166human GRCh37.p13 chr16: 28,479,999-28,646,000 , GRCh38.p12 chr16: 28,468,678-28,634,679 CLN3, SULT1A2, 7 more genes
    nsv4457062copy number variation1nstd102humanUncertain significance GRCh37 chr16: 28,466,730-28,585,574 , GRCh38.p12 chr16: 28,455,409-28,574,253 CLN3, APOBR, 4 more genes
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