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Items: 1 to 20 of 149

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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
    nsv5588676copy number variation1nstd207human GRCh38 chr16: 2,801,973-2,802,022 , GRCh37.p13 chr16: 2,851,974-2,852,023 PRSS41
    nsv5272285copy number variation1nstd204human GRCh38.p13 chr16: 2,651,201-3,235,500 , GRCh37.p13 chr16: 2,701,202-3,285,500 , RNU1-125P, 64 more genes
    nsv5269318copy number variation1nstd204human GRCh38.p13 chr16: 1,733,301-3,469,700 , GRCh37.p13 chr16: 1,783,302-3,519,700 , MIR6511B1, 156 more genes
    nsv5262390copy number variation1nstd204human GRCh38.p13 chr16: 2,578,401-2,889,000 , GRCh37.p13 chr16: 2,628,402-2,939,001 PRSS30P, ELOB, 18 more genes
    nsv4735089copy number variation1nstd199human GRCh37 chr16: 2,851,937-2,851,989 , GRCh38.p12 chr16: 2,801,936-2,801,988 PRSS41
    nsv4729241copy number variation1nstd102humanPathogenic GRCh37 chr16: 85,880-5,249,457 , GRCh38.p12 chr16: 35,880-5,199,456 MTRNR2L4, BRICD5, 307 more genes
    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
    nsv4576688mobile element insertion1nstd166human GRCh37.p13 chr16: 2,853,234-2,853,234 , GRCh38.p12 chr16: 2,803,233-2,803,233 PRSS41
    nsv4531159copy number variation1nstd166human GRCh37.p13 chr16: 2,852,102-2,852,458 , GRCh38.p12 chr16: 2,802,101-2,802,457 PRSS41
    nsv4510226mobile element insertion1nstd166human GRCh37.p13 chr16: 2,850,898-2,850,898 , GRCh38.p12 chr16: 2,800,897-2,800,897 PRSS41
    nsv4457303copy number variation1nstd102humanUncertain significance GRCh37 chr16: 2,716,924-3,055,626 , GRCh38.p12 chr16: 2,666,923-3,005,625 ELOB, PRSS21, 21 more genes
    nsv4456186copy number variation1nstd102humanUncertain significance GRCh37 chr16: 2,817,166-3,056,563 , GRCh38.p12 chr16: 2,767,165-3,006,562 PRSS33, SRRM2, 17 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
    nsv4365040copy number variation1nstd173human GRCh37 chr16: 2,805,634-3,224,098 , GRCh38.p12 chr16: 2,755,633-3,174,097 , TRR-CCT3-1, 48 more genes
    nsv4349832copy number variation1nstd102humanPathogenic GRCh37 chr16: 109,978-4,316,797 , GRCh38.p12 chr16: 59,980-4,266,796 LINC00235, RNF151, 269 more genes
    nsv3966199insertion1nstd168human GRCh38 chr16: 2,756,596-2,899,195 , GRCh37.p13 chr16: 2,806,597-2,949,196 SRRM2, PRSS30P, 10 more genes
    nsv3923267copy number variation1nstd102humanPathogenic GRCh37 chr16: 93,732-13,420,663 , GRCh38 chr16: 43,732-13,326,806 , NCBI36 chr16: 33,732-13,328,164 METRN, FAM234A, 413 more genes
    nsv3923184copy number variation1nstd102humanPathogenic GRCh37 chr16: 96,766-3,264,623 , GRCh38 chr16: 46,766-3,214,623 , NCBI36 chr16: 36,766-3,204,624 TRP-CGG1-2, HAGHL, 235 more genes
    nsv3922813copy number variation1nstd102humanUncertain significance GRCh38 chr16: 2,586,110-2,804,741 , NCBI36 chr16: 2,576,112-2,794,743 , GRCh37 chr16: 2,636,111-2,854,742 PRSS27, SNORA3C, 11 more genes
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