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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148136copy number variation1nstd102humanPathogenic GRCh37 chr14: 100,367,259-101,508,462 , GRCh38.p12 chr14: 99,900,922-101,042,125 SNORD113-5, SNORD114-27, 99 more genes
    nsv6973906copy number variation1nstd229human GRCh38 chr14: 100,735,892-100,772,269 , GRCh37.p13 chr14: 101,202,229-101,238,606 DLK1
    nsv6959979copy number variation1nstd229human GRCh38 chr14: 100,712,654-100,760,718 , GRCh37.p13 chr14: 101,178,991-101,227,055 DLK1
    nsv6958205copy number variation1nstd229human GRCh38 chr14: 100,548,933-100,726,606 , GRCh37.p13 chr14: 101,015,270-101,192,943 LOC105370669, BEGAIN, 3 more genes
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
    nsv6495845copy number variation1nstd223human GRCh38 chr14: 100,737,763-100,738,102 , GRCh37.p13 chr14: 101,204,100-101,204,439 DLK1
    nsv6495635copy number variation1nstd223human GRCh38 chr14: 100,548,933-100,726,606 , GRCh37.p13 chr14: 101,015,270-101,192,943 DLK1, LOC105370668, 3 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6291768copy number variation1nstd102humanPathogenic GRCh37 chr14: 95,871,795-102,457,523 , GRCh38.p12 chr14: 95,405,458-101,991,186 CCDC85C, MEG3, 206 more genes
    nsv6132885copy number variation1nstd213human GRCh37 chr14: 99,590,000-101,630,001 , GRCh38.p12 chr14: 99,123,663-101,163,664 DLK1, MEG8, 135 more genes
    nsv6036017copy number variation1nstd212human GRCh38 chr14: 100,737,027-100,737,098 , GRCh37.p13 chr14: 101,203,364-101,203,435 DLK1
    nsv5696003mobile element insertion1nstd211human GRCh38 chr14: 100,731,966-100,731,966 , GRCh37.p13 chr14: 101,198,303-101,198,303 DLK1
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5428264mobile element insertion1nstd206human GRCh38 chr14: 100,731,966-100,732,017 , GRCh37.p13 chr14: 101,198,303-101,198,354 DLK1
    nsv4991393copy number variation1nstd200human GRCh38 chr14: 100,725,643-100,725,775 , GRCh37.p13 chr14: 101,191,980-101,192,112 DLK1
    nsv4854979copy number variation1nstd200human GRCh37 chr14: 101,191,980-101,192,112 , GRCh38.p12 chr14: 100,725,643-100,725,775 DLK1
    nsv4728990copy number variation1nstd102humanPathogenic GRCh37 chr14: 101,201,380-101,290,903 , GRCh38.p12 chr14: 100,735,043-100,824,566 DLK1, MIR2392, 1 more genes
    nsv4684265copy number variation1nstd102humanPathogenic GRCh37 chr14: 96,829,290-107,287,663 , GRCh38.p12 chr14: 96,362,953-106,879,456 NDUFB3P4, LINC02320, 502 more genes
    nsv4456178copy number variation1nstd102humanPathogenic GRCh37 chr14: 91,969,028-107,285,437 , GRCh38.p12 chr14: 91,502,684-106,877,229 LOC105370639, SERPINA9, 600 more genes
    nsv4455156copy number variation1nstd102humanPathogenic GRCh37 chr14: 99,794,230-107,285,437 , GRCh38.p12 chr14: 99,327,893-106,877,229 IGHG4, IGHV3-57, 464 more genes
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