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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094498copy number variation1nstd102humanPathogenic GRCh37 chr14: 36,988,170-36,989,334 , GRCh38.p12 chr14: 36,518,965-36,520,129 SFTA3, NKX2-1-AS1, 1 more genes
    nsv6956783copy number variation1nstd229human GRCh38 chr14: 36,512,101-36,527,500 , GRCh37.p13 chr14: 36,981,306-36,996,705 NKX2-1, LOC105370453, 2 more genes
    nsv6941451copy number variation1nstd229human GRCh38 chr14: 36,516,745-36,517,316 , GRCh37.p13 chr14: 36,985,950-36,986,521 NKX2-1-AS1, NKX2-1, 1 more genes
    nsv6622519copy number variation1nstd224human GRCh37 chr14: 36,916,520-37,243,034 , GRCh38.p12 chr14: 36,447,315-36,773,829 PAX9, SLC25A21, 9 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
    nsv6313989copy number variation1nstd102humanUncertain significance GRCh37 chr14: 36,924,877-37,247,672 , GRCh38.p12 chr14: 36,455,672-36,778,467 NKX2-8, PAX9, 9 more genes
    nsv6313950copy number variation1nstd102humanUncertain significance GRCh37 chr14: 36,933,561-37,247,672 , GRCh38.p12 chr14: 36,464,356-36,778,467 NKX2-1, RPL29P3, 9 more genes
    nsv6313916copy number variation1nstd102humanPathogenic GRCh37 chr14: 36,862,276-41,597,549 , GRCh38.p12 chr14: 36,393,071-41,128,344 LOC105370462, LOC105370459, 55 more genes
    nsv6309692copy number variation1nstd102humanPathogenic GRCh37 chr14: 36,986,483-36,987,245 , GRCh38.p12 chr14: 36,517,278-36,518,040 NKX2-1, SFTA3, 1 more genes
    nsv6309545copy number variation1nstd102humanUncertain significance GRCh37 chr14: 36,986,483-37,228,504 , GRCh38.p12 chr14: 36,517,278-36,759,299 LOC105370455, PHKBP2, 9 more genes
    nsv6133125copy number variation1nstd213human GRCh37 chr14: 36,260,000-37,190,001 , GRCh38.p12 chr14: 35,790,794-36,720,796 MBIP, LOC644584, 22 more genes
    nsv6106211inversion1nstd212human GRCh38 chr14: 35,414,234-38,834,329 , GRCh37.p13 chr14: 35,883,440-39,303,533 , FOXA1, 49 more genes
    nsv5498015copy number variation1nstd206human GRCh38 chr14: 34,191,713-38,057,713 , GRCh37.p13 chr14: 34,660,919-38,526,918 , RPL23AP71, 79 more genes
    nsv5381757copy number variation1nstd102humanPathogenic GRCh37 chr14: 33,608,925-44,570,367 , GRCh38.p12 chr14: 33,139,719-44,101,164 RPLP0P3, KRT18P6, 131 more genes
    nsv4994208copy number variation1nstd200human GRCh38 chr14: 36,445,089-36,783,320 , GRCh37.p13 chr14: 36,914,294-37,252,525 PHKBP2, LOC105370453, 9 more genes
    nsv4729151copy number variation1nstd102humanPathogenic GRCh37 chr14: 36,969,461-37,264,529 , GRCh38.p12 chr14: 36,500,256-36,795,324 PHKBP2, LOC105370455, 9 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
    nsv4676032copy number variation1nstd102humanPathogenic GRCh37 chr14: 36,830,396-42,541,277 , GRCh38.p12 chr14: 36,361,190-42,072,074 PPIAP4, LOC100533628, 60 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
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