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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6129243mobile element insertion1nstd186human GRCh37 chr14: 20,615,847-20,615,885 , GRCh38.p12 chr14: 20,147,688-20,147,726 PSMB7P1
    nsv5976014insertion1nstd209human GRCh38 chr14: 20,147,688-20,147,688 , GRCh37.p13 chr14: 20,615,847-20,615,847 PSMB7P1
    nsv5943393copy number variation1nstd209human GRCh38 chr14: 20,038,752-20,231,884 , GRCh37.p13 chr14: 20,506,911-20,700,043 PSMB7P1, OR11G2, 12 more genes
    nsv5728452mobile element insertion2nstd211human GRCh38 chr14: 20,147,675-20,147,675 , GRCh37.p13 chr14: 20,615,834-20,615,834 PSMB7P1
    nsv5659187insertion1nstd207human GRCh38 chr14: 20,147,688-20,147,688 , GRCh37.p13 chr14: 20,615,847-20,615,847 PSMB7P1
    nsv5554971mobile element insertion1nstd206human GRCh38 chr14: 20,147,688-20,147,726 , GRCh37.p13 chr14: 20,615,847-20,615,885 PSMB7P1
    nsv5349018translocation1nstd200human GRCh38 chr14: 20,148,874-20,148,874 , GRCh38 chr14: 20,148,953-20,148,953 , GRCh37.p13 chr14: 20,617,033-20,617,033 , GRCh37.p13 chr14: 20,617,112-20,617,112 PSMB7P1
    nsv5186500mobile element insertion1nstd203human GRCh38 chr14: 20,147,675-20,147,675 , GRCh37.p13 chr14: 20,615,834-20,615,834 PSMB7P1
    nsv5185001mobile element insertion1nstd203human GRCh38 chr14: 20,147,680-20,147,680 , GRCh37.p13 chr14: 20,615,839-20,615,839 PSMB7P1
    nsv4994067copy number variation1nstd200human GRCh38 chr14: 20,067,185-20,201,105 , GRCh37.p13 chr14: 20,535,344-20,669,264 OR4N5, OR11P1P, 7 more genes
    nsv4994063copy number variation1nstd200human GRCh38 chr14: 20,013,868-20,436,718 , GRCh37.p13 chr14: 20,482,027-20,904,877 OR4K17, OR4L1, 25 more genes
    nsv4750286insertion1nstd199human GRCh37 chr14: 20,615,844-20,615,844 , GRCh38.p12 chr14: 20,147,685-20,147,685 PSMB7P1
    nsv4729394copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-21,915,516 , GRCh38.p12 chr14: 20,043,513-21,447,357 SETP1, OR11H5P, 99 more genes
    nsv4726614mobile element insertion1nstd186human GRCh37 chr14: 20,615,834-20,615,834 , GRCh38.p12 chr14: 20,147,675-20,147,675 PSMB7P1
    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
    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
    nsv4574221mobile element insertion1nstd166human GRCh37.p13 chr14: 20,615,834-20,615,834 , GRCh38.p12 chr14: 20,147,675-20,147,675 PSMB7P1
    nsv4455321copy number variation1nstd102humanUncertain significance GRCh37 chr14: 20,511,672-21,174,548 , GRCh38.p12 chr14: 20,043,513-20,706,389 PARP2, TRL-AAG2-3, 53 more genes
    nsv4455170copy number variation1nstd102humanUncertain significance GRCh37 chr14: 20,511,672-20,903,963 , GRCh38.p12 chr14: 20,043,513-20,435,804 OR11G2, KLHL33, 22 more genes
    nsv4417741copy number variation1nstd174human GRCh37 chr14: 20,511,673-20,698,504 , GRCh38.p12 chr14: 20,043,514-20,230,345 OR4U1P, OR4N5, 12 more genes
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