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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5945341copy number variation1nstd209human GRCh38 chr15: 38,282,856-38,282,972 , GRCh37.p13 chr15: 38,575,057-38,575,173 SPRED1
    nsv5939106copy number variation1nstd209human GRCh38 chr15: 38,008,106-40,186,655 , GRCh37.p13 chr15: 38,300,307-40,478,856 , LOC105370784, 36 more genes
    nsv5937394copy number variation1nstd209human GRCh38 chr15: 38,284,565-38,284,663 , GRCh37.p13 chr15: 38,576,766-38,576,864 SPRED1
    nsv5726097mobile element insertion1nstd211human GRCh38 chr15: 38,318,184-38,318,184 , GRCh37.p13 chr15: 38,610,385-38,610,385 SPRED1
    nsv5672738copy number variation1nstd102humanPathogenic GRCh37 chr15: 38,591,568-38,643,870 , GRCh38.p12 chr15: 38,299,367-38,351,669 SPRED1
    nsv5672664copy number variation1nstd102humanPathogenic GRCh37 chr15: 38,545,367-38,545,438 , GRCh38.p12 chr15: 38,253,166-38,253,237 SPRED1
    nsv5505735copy number variation1nstd206human GRCh38 chr15: 38,353,566-38,353,635 , GRCh37.p13 chr15: 38,645,767-38,645,836 SPRED1
    nsv5505197copy number variation1nstd206human GRCh38 chr15: 38,318,095-38,319,114 , GRCh37.p13 chr15: 38,610,296-38,611,315 SPRED1
    nsv5494689copy number variation1nstd206human GRCh38 chr15: 38,282,856-38,282,973 , GRCh37.p13 chr15: 38,575,057-38,575,174 SPRED1
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv5180696mobile element insertion1nstd203human GRCh38 chr15: 38,318,171-38,318,184 , GRCh37.p13 chr15: 38,610,372-38,610,385 SPRED1
    nsv5001306copy number variation1nstd200human GRCh38 chr15: 38,290,744-38,290,794 , GRCh37.p13 chr15: 38,582,945-38,582,995 SPRED1
    nsv5001305copy number variation1nstd200human GRCh38 chr15: 38,282,856-38,282,973 , GRCh37.p13 chr15: 38,575,057-38,575,174 SPRED1
    nsv4855898copy number variation1nstd200human GRCh37 chr15: 38,635,438-38,635,528 , GRCh38.p12 chr15: 38,343,237-38,343,327 SPRED1
    nsv4855897copy number variation1nstd200human GRCh37 chr15: 38,575,057-38,575,174 , GRCh38.p12 chr15: 38,282,856-38,282,973 SPRED1
    nsv4855793copy number variation1nstd200human GRCh37 chr15: 34,109,797-39,904,401 , GRCh38.p12 chr15: 33,817,596-39,612,200 , AQR, 87 more genes
    nsv4729292copy number variation1nstd102humanUncertain significance GRCh37 chr15: 38,632,117-39,790,989 , GRCh38.p12 chr15: 38,339,916-39,498,788 LOC102724253, FAM98B, 12 more genes
    nsv4683193copy number variation1nstd102humanPathogenic GRCh37 chr15: 38,591,564-38,617,020 , GRCh38.p12 chr15: 38,299,363-38,324,819 SPRED1
    nsv4675391copy number variation1nstd102humanPathogenic GRCh37 chr15: 34,197,488-38,656,254 , GRCh38.p12 chr15: 33,905,287-38,364,053 TPST2P1, AVEN, 65 more genes
    nsv4633245copy number variation1nstd183human GRCh37 chr15: 38,648,257-38,654,980 , GRCh38.p12 chr15: 38,356,056-38,362,779 SPRED1
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