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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148188copy number variation1nstd102humanPathogenic GRCh38 chr5: 88,189,536-93,784,597 , GRCh37.p13 chr5: 87,485,353-93,120,303 RPS3AP22, LOC105379078, 49 more genes
    nsv7147131insertion1nstd232human GRCh37.p13 chr5: 89,689,924-89,689,924 , GRCh38.p12 chr5: 90,394,107-90,394,107 CETN3
    nsv7144545insertion1nstd232human GRCh37.p13 chr5: 89,695,369-89,695,369 , GRCh38.p12 chr5: 90,399,552-90,399,552 CETN3
    nsv7051643inversion1nstd229human GRCh38 chr5: 89,525,249-90,520,207 , GRCh37.p13 chr5: 88,821,066-89,816,024 CETN3, LOC731157, 7 more genes
    nsv6634473inversion1nstd102humanPathogenic GRCh37 chr5: 88,625,195-90,796,047 , GRCh38.p12 chr5: 89,329,378-91,500,230 CETN3, POLR3G, 22 more genes
    nsv6408827copy number variation1nstd223human GRCh38 chr5: 90,394,148-90,394,570 , GRCh37.p13 chr5: 89,689,965-89,690,387 CETN3
    nsv6401080copy number variation1nstd223human GRCh38 chr5: 90,409,144-90,413,140 , GRCh37.p13 chr5: 89,704,961-89,708,957 LOC731157, CETN3
    nsv6396940copy number variation1nstd223human GRCh38 chr5: 90,393,401-90,394,900 , GRCh37.p13 chr5: 89,689,218-89,690,717 CETN3
    nsv6313788copy number variation1nstd102humanPathogenic GRCh37 chr5: 82,185,951-90,110,454 , GRCh38.p12 chr5: 82,890,132-90,814,637 RASA1, HAPLN1, 82 more genes
    nsv6135685copy number variation1nstd213human GRCh37 chr5: 87,880,000-90,240,001 , GRCh38.p12 chr5: 88,584,182-90,944,184 CETN3, MEF2C, 18 more genes
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
    nsv6135200copy number variation1nstd213human GRCh37 chr5: 76,540,000-94,260,001 , GRCh38.p12 chr5: 77,244,175-94,924,296 ACTBP2, ARSB, 200 more genes
    nsv5685690mobile element insertion2nstd211human GRCh38 chr5: 90,406,692-90,406,692 , GRCh37.p13 chr5: 89,702,509-89,702,509 CETN3
    nsv5400652mobile element insertion1nstd206human GRCh38 chr5: 90,406,692-90,406,743 , GRCh37.p13 chr5: 89,702,509-89,702,560 CETN3
    nsv5097683mobile element insertion1nstd203human GRCh38 chr5: 90,406,840-90,406,840 , GRCh37.p13 chr5: 89,702,657-89,702,657 CETN3
    nsv5084071mobile element insertion1nstd203human GRCh38 chr5: 90,406,682-90,406,692 , GRCh37.p13 chr5: 89,702,499-89,702,509 CETN3
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4947135copy number variation1nstd200human GRCh38 chr5: 90,409,144-90,413,140 , GRCh37.p13 chr5: 89,704,961-89,708,957 LOC731157, CETN3
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
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