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Items: 1 to 20 of 127

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094423copy number variation2nstd102humanUncertain significance GRCh37 chr14: 23,242,819-25,103,366 , GRCh38.p12 chr14: 22,773,610-24,634,160 LINC00596, NGDN, 107 more genes
    nsv7077744inversion1nstd229human GRCh38 chr14: 23,524,700-23,527,373 , GRCh37.p13 chr14: 23,993,909-23,996,582 THTPA, ZFHX2
    nsv7074310inversion1nstd229human GRCh38 chr14: 22,076,285-27,854,954 , GRCh37.p13 chr14: 22,544,546-28,324,160 PPP1R3E, TRAJ37, 242 more genes
    nsv7066614inversion1nstd229human GRCh38 chr14: 23,512,314-23,521,048 , GRCh37.p13 chr14: 23,981,523-23,990,257 ZFHX2, THTPA
    nsv7059682inversion1nstd229human GRCh38 chr14: 23,532,516-23,539,446 , GRCh37.p13 chr14: 24,001,725-24,008,655 ZFHX2, THTPA
    nsv6957760copy number variation1nstd229human GRCh38 chr14: 23,359,284-23,513,241 , GRCh37.p13 chr14: 23,828,493-23,982,450 MYH6, EFS, 8 more genes
    nsv6957171copy number variation1nstd229human GRCh38 chr14: 23,494,201-23,604,800 , GRCh37.p13 chr14: 23,963,410-24,074,009 AP1G2, ZFHX2, 3 more genes
    nsv6955004copy number variation1nstd229human GRCh38 chr14: 23,542,537-23,546,558 , GRCh37.p13 chr14: 24,011,746-24,015,767 ZFHX2, THTPA
    nsv6942851copy number variation1nstd229human GRCh38 chr14: 23,531,887-23,542,880 , GRCh37.p13 chr14: 24,001,096-24,012,089 THTPA, ZFHX2
    nsv6939312copy number variation1nstd229human GRCh38 chr14: 23,547,583-23,548,158 , GRCh37.p13 chr14: 24,016,792-24,017,367 ZFHX2, THTPA
    nsv6477433copy number variation1nstd223human GRCh38 chr14: 23,544,752-23,552,762 , GRCh37.p13 chr14: 24,013,961-24,021,971 ZFHX2, THTPA
    nsv6476778copy number variation1nstd223human GRCh38 chr14: 23,542,537-23,546,556 , GRCh37.p13 chr14: 24,011,746-24,015,765 ZFHX2, THTPA
    nsv6315513copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000 CDH24, KLHL33, 623 more genes
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 HNRNPC, FOXG1, 616 more genes
    nsv6132775copy number variation1nstd213human GRCh37 chr14: 22,590,000-24,410,001 , GRCh38.p12 chr14: 22,122,042-23,940,792 BCL2L2, CEBPE, 167 more genes
    nsv5943425copy number variation1nstd209human GRCh38 chr14: 23,553,338-23,553,632 , GRCh37.p13 chr14: 24,022,547-24,022,841 ZFHX2, THTPA
    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
    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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