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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
    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
    nsv7070619inversion1nstd229human GRCh38 chr14: 23,713,943-24,501,695 , GRCh37.p13 chr14: 24,183,152-24,970,901 TSSK4, RIPK3, 48 more genes
    nsv6947120copy number variation1nstd229human GRCh38 chr14: 24,051,966-24,052,010 , GRCh37.p13 chr14: 24,521,175-24,521,219 CARMIL3
    nsv6941402copy number variation1nstd229human GRCh38 chr14: 24,059,301-24,305,100 , GRCh37.p13 chr14: 24,528,510-24,774,306 PSME2, CIDEB, 27 more genes
    nsv6938849copy number variation1nstd229human GRCh38 chr14: 24,066,252-24,067,126 , GRCh37.p13 chr14: 24,535,461-24,536,335 CARMIL3, LOC105370412
    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
    nsv6132776copy number variation1nstd213human GRCh37 chr14: 24,490,000-28,000,001 , GRCh38.p12 chr14: 24,020,791-27,530,795 CMA1, LTB4R, 65 more genes
    nsv5263479copy number variation1nstd204human GRCh38.p13 chr14: 24,019,501-24,275,100 , GRCh37.p13 chr14: 24,488,710-24,744,306 , RABGGTA, 26 more genes
    nsv4728842copy number variation1nstd102humanUncertain significance GRCh37 chr14: 24,163,771-24,818,728 , GRCh38.p12 chr14: 23,694,562-24,347,428 , GRCh38.p12 chr14|NW_018654722.1: 1-650,500 FITM1, CIDEB, 44 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
    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
    nsv4620540copy number variation1nstd183human GRCh37 chr14: 24,520,449-24,521,251 , GRCh38.p12 chr14: 24,051,240-24,052,042 , GRCh38.p12 chr14|NW_018654722.1: 352,218-353,020 CARMIL3, DHRS4L1
    nsv4578623copy number variation1nstd102humanUncertain significance GRCh37 chr14: 24,505,708-24,601,038 , GRCh38.p12 chr14: 24,036,499-24,131,829 , GRCh38.p12 chr14|NW_018654722.1: 337,477-432,807 CPNE6, LOC105370412, 6 more genes
    nsv4424538copy number variation1nstd174human GRCh37 chr14: 24,503,854-24,523,979 , GRCh38.p12 chr14: 24,034,645-24,054,770 , GRCh38.p12 chr14|NW_018654722.1: 335,623-355,748 CARMIL3, DHRS4L1
    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
    nsv4222413copy number variation1nstd166human GRCh37.p13 chr14: 24,485,800-24,520,300 , GRCh38.p12 chr14|NW_018654722.1: 334,305-352,069 , GRCh38.p12 chr14: 24,033,327-24,051,091 CARMIL3, DHRS4L1
    nsv3922265copy number variation1nstd102humanLikely pathogenic NCBI36 chr14: 19,950,586-24,557,166 , GRCh37 chr14: 20,880,746-25,487,326 , GRCh38 chr14: 20,412,587-25,018,120 ANG, APEX1, 346 more genes
    nsv3919655copy number variation1nstd102humanPathogenic GRCh37 chr14: 24,453,274-25,843,700 , GRCh38 chr14: 23,984,065-25,374,494 , NCBI36 chr14: 23,523,114-24,913,540 NFATC4, LTB4R, 50 more genes
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