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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148126copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,851,693-22,089,506 , GRCh38.p12 chr14: 21,383,534-21,621,353 OR10G3, SNORD9, 17 more genes
    nsv7147958insertion1nstd232human GRCh37.p13 chr14: 21,966,516-21,966,516 , GRCh38.p12 chr14: 21,498,372-21,498,372 TOX4, METTL3
    nsv7143164copy number variation1nstd232human GRCh37.p13 chr14: 21,971,720-21,971,805 , GRCh38.p12 chr14: 21,503,577-21,503,662 METTL3
    nsv7139680insertion1nstd232human GRCh37.p13 chr14: 21,969,274-21,969,274 , GRCh38.p12 chr14: 21,501,132-21,501,132 METTL3
    nsv7094421copy number variation1nstd102humanUncertain significance GRCh37 chr14: 21,671,278-22,005,055 , GRCh38.p12 chr14: 21,203,119-21,536,921 RN7SL650P, SNORD9, 14 more genes
    nsv7094244copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,915,399-22,005,055 , GRCh38.p12 chr14: 20,447,240-21,536,921 ARHGEF40, LOC105370398, 78 more genes
    nsv7072621inversion1nstd229human GRCh38 chr14: 20,991,576-21,885,954 , GRCh37.p13 chr14: 21,459,735-22,354,136 LINC00641, TRAV13-1, 61 more genes
    nsv7066014inversion1nstd229human GRCh38 chr14: 21,507,747-21,507,816 , GRCh37.p13 chr14: 21,975,889-21,975,958 METTL3
    nsv6950128copy number variation1nstd229human GRCh38 chr14: 21,498,965-21,499,432 , GRCh37.p13 chr14: 21,967,109-21,967,576 METTL3, TOX4
    nsv6945492copy number variation1nstd229human GRCh38 chr14: 21,499,663-21,505,584 , GRCh37.p13 chr14: 21,967,807-21,973,726 METTL3, TOX4
    nsv6637318copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,690,196-23,114,522 , GRCh38.p12 chr14: 20,222,037-22,645,313 TRAJ21, TRAJ44, 239 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
    nsv6290276copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 20,925,965-23,649,548 , GRCh38.p12 chr14: 20,457,806-23,180,339 ANG, APEX1, 255 more genes
    nsv6132583copy number variation1nstd213human GRCh37 chr14: 20,420,000-22,590,001 , GRCh38.p12 chr14: 19,951,841-22,122,043 HNRNPC, PNP, 157 more genes
    nsv5672730copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,756,136-22,005,055 , GRCh38.p12 chr14: 21,287,977-21,536,921 RAB2B, METTL3, 12 more genes
    nsv5506506copy number variation1nstd206human GRCh38 chr14: 21,455,390-21,561,947 , GRCh37.p13 chr14: 21,923,549-22,030,078 SALL2, TOX4, 4 more genes
    nsv4756777insertion1nstd199human GRCh37 chr14: 21,974,206-21,974,206 , GRCh38.p12 chr14: 21,506,064-21,506,064 METTL3
    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
    nsv4676085copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,143,933-23,297,667 , GRCh38.p12 chr14: 20,675,774-22,828,458 ANG, SNORD8, 209 more genes
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