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Items: 1 to 20 of 73

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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
    nsv5968990insertion1nstd209human GRCh38 chr16: 4,739,265-4,739,265 , GRCh37.p13 chr16: 4,789,266-4,789,266 DNAAF8
    nsv5529627copy number variation1nstd206human GRCh38 chr16: 4,735,868-4,738,335 , GRCh37.p13 chr16: 4,785,869-4,788,336 DNAAF8
    nsv5365489translocation1nstd200human GRCh38 chr16: 4,735,390-4,735,390 , GRCh38 chr16: 4,727,880-4,727,880 , GRCh37.p13 chr16: 4,785,391-4,785,391 , GRCh37.p13 chr16: 4,777,881-4,777,881 DNAAF8, ANKS3
    nsv5270826copy number variation1nstd204human GRCh38.p13 chr16: 4,289,501-4,742,300 , GRCh37.p13 chr16: 4,339,502-4,792,301 HMOX2, NMRAL1, 17 more genes
    nsv5009401copy number variation1nstd200human GRCh38 chr16: 4,700,207-4,771,275 , GRCh37.p13 chr16: 4,750,208-4,821,276 DNAAF8, ANKS3, 1 more genes
    nsv5008116copy number variation1nstd200human GRCh38 chr16: 4,732,537-5,127,796 , GRCh37.p13 chr16: 4,782,538-5,177,797 NAGPA, PPL, 16 more genes
    nsv4866532copy number variation1nstd200human GRCh37 chr16: 4,750,181-4,820,744 , GRCh38.p12 chr16: 4,700,180-4,770,743 ZNF500, ANKS3, 1 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
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
    nsv4683689copy number variation1nstd102humanUncertain significance GRCh37 chr16: 3,777,699-4,852,592 , GRCh38.p12 chr16: 3,727,698-4,802,591 UBALD1, HMOX2, 30 more genes
    nsv4623929copy number variation1nstd183human GRCh37 chr16: 4,785,869-4,788,336 , GRCh38.p12 chr16: 4,735,868-4,738,335 DNAAF8
    nsv4574049mobile element insertion1nstd166human GRCh37.p13 chr16: 4,794,530-4,794,530 , GRCh38.p12 chr16: 4,744,529-4,744,529 DNAAF8, ZNF500
    nsv4550362insertion1nstd166human GRCh37.p13 chr16: 4,791,625-4,791,625 , GRCh38.p12 chr16: 4,741,624-4,741,624 DNAAF8
    nsv4510328mobile element insertion1nstd166human GRCh37.p13 chr16: 4,787,579-4,787,579 , GRCh38.p12 chr16: 4,737,578-4,737,578 DNAAF8
    nsv4456218copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,731,117-5,325,699 , GRCh38.p12 chr16: 3,681,116-5,275,698 CORO7-PAM16, DBIP3, 46 more genes
    nsv4453988copy number variation1nstd102humanPathogenic GRCh38 chr16: 3,727,698-4,802,591 , GRCh37 chr16: 3,777,699-4,852,592 RN7SL850P, ZNF500, 30 more genes
    nsv4436312complex substitution1nstd102humanPathogenic GRCh38.p12 chr16: 1,230,041-33,908,091 , GRCh37 chr16: 1,280,042-33,710,558 ABAT, ABCA3, 876 more genes
    nsv4249461copy number variation1nstd166human GRCh37.p13 chr16: 4,767,930-4,859,302 , GRCh38.p12 chr16: 4,717,929-4,809,301 ZNF500, ROGDI, 5 more genes
    nsv4249333copy number variation1nstd166human GRCh37.p13 chr16: 4,767,000-4,827,500 , GRCh38.p12 chr16: 4,716,999-4,777,499 SEPTIN12, ZNF500, 2 more genes
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