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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5645306insertion1nstd207human GRCh38 chr14: 23,422,574-23,422,574 , GRCh37.p13 chr14: 23,891,783-23,891,783 MYH7
    nsv5564380copy number variation2nstd102humanUncertain significance GRCh37 chr14: 23,861,761-23,889,453 , GRCh38.p12 chr14: 23,392,552-23,420,244 MYH6, MYH7, 2 more genes
    nsv5380968copy number variation1nstd102humanUncertain significance GRCh37 chr14: 23,856,957-23,886,537 , GRCh38.p12 chr14: 23,387,748-23,417,328 MIR208A, MYH6, 3 more genes
    nsv5380913copy number variation1nstd102humanUncertain significance GRCh37 chr14: 23,898,144-23,899,892 , GRCh38.p12 chr14: 23,428,935-23,430,683 MYH7
    nsv5380828copy number variation1nstd102humanUncertain significance GRCh37 chr14: 23,885,203-23,885,531 , GRCh38.p12 chr14: 23,415,994-23,416,322 MYH7, MIR208B, 1 more genes
    nsv5380752copy number variation1nstd102humanUncertain significance GRCh37 chr14: 23,856,728-23,885,531 , GRCh38.p12 chr14: 23,387,519-23,416,322 MYH6, MIR208A, 3 more genes
    nsv4994113copy number variation1nstd200human GRCh38 chr14: 23,385,943-23,415,802 , GRCh37.p13 chr14: 23,855,152-23,885,011 MIR208A, MYH6, 2 more genes
    nsv4836592copy number variation1nstd200human GRCh37 chr14: 23,855,152-23,885,011 , GRCh38.p12 chr14: 23,385,943-23,415,802 MHRT, MYH7, 2 more genes
    nsv4685750copy number variation1nstd102humannot provided GRCh37 chr14: 20,511,672-42,881,888 , GRCh38.p12 chr14: 20,043,513-42,412,685 IGBP1P1, RAB2B, 579 more genes
    nsv4683851copy number variation2nstd102humanUncertain significance GRCh37 chr14: 23,861,761-23,888,828 , GRCh38.p12 chr14: 23,392,552-23,419,619 MIR208B, MHRT, 2 more genes
    nsv4683784copy number variation1nstd102humanUncertain significance GRCh37 chr14: 23,857,354-23,886,537 , GRCh38.p12 chr14: 23,388,145-23,417,328 MYH7, MHRT, 3 more genes
    nsv4683221copy number variation2nstd102humanUncertain significance GRCh37 chr14: 23,856,728-23,885,051 , GRCh38.p12 chr14: 23,387,519-23,415,842 MYH6, MYH7, 2 more genes
    nsv4682937copy number variation1nstd102humanUncertain significance GRCh37 chr14: 23,859,256-23,889,453 , GRCh38.p12 chr14: 23,390,047-23,420,244 MIR208B, MYH7, 2 more genes
    nsv4681884copy number variation1nstd102humanUncertain significance GRCh37 chr14: 23,897,769-23,900,067 , GRCh38 chr14: 23,428,560-23,430,858 MYH7
    nsv4681406copy number variation1nstd102humanUncertain significance GRCh37 chr14: 23,851,239-23,903,456 , GRCh38.p12 chr14: 23,382,030-23,434,247 MHRT, MIR208A, 3 more genes
    nsv4681283copy number variation1nstd102humanUncertain significance GRCh37 chr14: 23,882,063-23,889,453 , GRCh38.p12 chr14: 23,412,854-23,420,244 MYH7, MHRT, 1 more genes
    nsv4675943copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-44,829,030 , GRCh38.p12 chr14: 20,043,513-44,359,827 TRAJ36, SEC23A-AS1, 590 more genes
    nsv4619650copy number variation1nstd183human GRCh37 chr14: 23,900,887-23,900,942 , GRCh38.p12 chr14: 23,431,678-23,431,733 MYH7
    nsv4578270copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 21,717,093-24,027,220 , GRCh38.p12 chr14: 21,248,934-23,558,011 BCL2L2, CEBPE, 215 more genes
    nsv4349901copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,100,682-28,730,087 , GRCh38.p12 chr14: 18,324,205-28,260,881 TRAV4, UNGP2, 458 more genes
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