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Items: 1 to 20 of 97

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094491copy number variation1nstd102humanPathogenic GRCh37 chr14: 23,586,696-23,902,941 , GRCh38.p12 chr14: 23,117,487-23,433,732 SLC22A17, CMTM5, 21 more genes
    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
    nsv7074310inversion1nstd229human GRCh38 chr14: 22,076,285-27,854,954 , GRCh37.p13 chr14: 22,544,546-28,324,160 PPP1R3E, TRAJ37, 242 more genes
    nsv6952014copy number variation1nstd229human GRCh38 chr14: 23,247,096-23,376,847 , GRCh37.p13 chr14: 23,716,305-23,846,056 HOMEZ, RNU6-1046P, 11 more genes
    nsv6949077copy number variation1nstd229human GRCh38 chr14: 23,085,796-23,343,864 , GRCh37.p13 chr14: 23,555,005-23,813,073 RNU6-1138P, H3P37, 15 more genes
    nsv6945698copy number variation1nstd229human GRCh38 chr14: 23,281,701-23,431,900 , GRCh37.p13 chr14: 23,750,910-23,901,109 BCL2L2, SLC22A17, 13 more genes
    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
    nsv6313998copy number variation1nstd102humanUncertain significance GRCh37 chr14: 23,590,841-23,823,265 , GRCh38.p12 chr14: 23,121,632-23,354,056 SLC7A8, PPP1R3E, 12 more genes
    nsv6249681mobile element insertion1nstd215human GRCh38 chr14: 23,295,313-23,295,313 , GRCh37.p13 chr14: 23,764,522-23,764,522 H3P37, PPP1R3E
    nsv6143201copy number variation1nstd206human GRCh38 chr14: 23,289,713-23,319,713 , GRCh37.p13 chr14: 23,758,922-23,788,922 BCL2L2, PPP1R3E, 3 more genes
    nsv6132862copy number variation1nstd213human GRCh37 chr14: 23,180,000-23,940,001 , GRCh38.p12 chr14: 22,710,791-23,470,792 BCL2L2, CEBPE, 47 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
    nsv6094444insertion1nstd212human GRCh38 chr14: 23,295,601-23,295,601 , GRCh37.p13 chr14: 23,764,810-23,764,810 PPP1R3E, H3P37
    nsv5943065copy number variation1nstd209human GRCh38 chr14: 23,300,158-23,300,501 , GRCh37.p13 chr14: 23,769,367-23,769,710 PPP1R3E
    nsv5713590mobile element insertion1nstd211human GRCh38 chr14: 23,303,010-23,303,010 , GRCh37.p13 chr14: 23,772,219-23,772,219 PPP1R3E
    nsv5698679mobile element insertion1nstd211human GRCh38 chr14: 23,295,608-23,295,608 , GRCh37.p13 chr14: 23,764,817-23,764,817 H3P37, PPP1R3E
    nsv5646739insertion1nstd207human GRCh38 chr14: 23,301,429-23,301,429 , GRCh37.p13 chr14: 23,770,638-23,770,638 PPP1R3E
    nsv5505902copy number variation1nstd206human GRCh38 chr14: 23,301,429-23,301,545 , GRCh37.p13 chr14: 23,770,638-23,770,754 PPP1R3E
    nsv5424408mobile element insertion1nstd206human GRCh38 chr14: 23,295,608-23,295,659 , GRCh37.p13 chr14: 23,764,817-23,764,868 H3P37, PPP1R3E
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