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Items: 1 to 20 of 138

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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
    nsv5529678copy number variation1nstd206human GRCh38 chr16: 2,837,597-2,837,707 , GRCh37.p13 chr16: 2,887,598-2,887,708 PRSS30P
    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
    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
    nsv4672437copy number variation1nstd186human GRCh37 chr16: 2,881,489-2,887,882 , GRCh38.p12 chr16: 2,831,488-2,837,881 , GRCh38.p12 chr16|NW_013171812.1: 10,953-17,343 ZG16B, PRSS30P
    nsv4625070copy number variation1nstd183human GRCh37 chr16: 2,881,489-2,887,882 , GRCh38.p12 chr16: 2,831,488-2,837,881 , GRCh38.p12 chr16|NW_013171812.1: 10,953-17,343 PRSS30P, ZG16B
    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
    nsv4455790copy number variation1nstd102humanUncertain significance GRCh37 chr16: 2,859,583-3,056,563 , GRCh38.p12 chr16: 2,809,582-3,006,562 KREMEN2, PRSS30P, 12 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
    nsv3919498copy number variation1nstd102humanUncertain significance NCBI36 chr16: 2,776,225-2,903,721 , GRCh37 chr16: 2,836,224-2,963,720 , GRCh38 chr16: 2,786,223-2,913,719 PRSS33, LOC101929566, 9 more genes
    nsv3917929copy number variation1nstd102humanPathogenic GRCh37 chr16: 96,766-11,619,372 , GRCh38 chr16: 46,766-11,525,516 , NCBI36 chr16: 36,766-11,526,873 LOC100130283, PGP, 386 more genes
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