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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5977937insertion1nstd209human GRCh38 chr19: 50,336,105-50,336,105 , GRCh37.p13 chr19: 50,839,362-50,839,362 LOC105372437, NAPSB
    nsv5974464inversion1nstd209human GRCh38 chr19: 49,769,209-52,432,690 , GRCh37.p13 chr19: 50,272,466-52,935,943 , AP2A1, 172 more genes
    nsv5970571inversion1nstd209human GRCh38 chr19: 50,142,503-50,623,829 , GRCh37.p13 chr19: 50,645,760-51,127,086 KCNC3, MYBPC2, 16 more genes
    nsv5530308copy number variation1nstd206human GRCh38 chr19: 50,337,594-50,341,776 , GRCh37.p13 chr19: 50,840,851-50,845,033 NAPSB, LOC105372437
    nsv5323763copy number variation1nstd204human GRCh37.p13 chr19: 50,840,633-50,865,226 , GRCh38.p13 chr19: 50,337,376-50,361,969 NAPSA, NAPSB, 1 more genes
    nsv5296384copy number variation1nstd204human GRCh38.p13 chr19: 50,338,730-50,362,070 , GRCh37.p13 chr19: 50,841,987-50,865,327 NAPSB, NAPSA, 1 more genes
    nsv5289680copy number variation1nstd204human GRCh38.p13 chr19: 50,337,401-50,362,000 , GRCh37.p13 chr19: 50,840,658-50,865,257 NAPSA, LOC105372437, 1 more genes
    nsv5175179mobile element insertion1nstd203human GRCh38 chr19: 50,344,936-50,344,942 , GRCh37.p13 chr19: 50,848,193-50,848,199 LOC105372437, NAPSB
    nsv5162830mobile element insertion1nstd203human GRCh38 chr19: 50,344,930-50,344,942 , GRCh37.p13 chr19: 50,848,187-50,848,199 NAPSB, LOC105372437
    nsv5024822copy number variation1nstd200human GRCh38 chr19: 50,338,742-50,339,508 , GRCh37.p13 chr19: 50,841,999-50,842,765 LOC105372437, NAPSB
    nsv5021037copy number variation1nstd200human GRCh38 chr19: 50,343,976-50,346,331 , GRCh37.p13 chr19: 50,847,233-50,849,588 NAPSB, LOC105372437
    nsv5021036copy number variation1nstd200human GRCh38 chr19: 50,339,369-50,341,224 , GRCh37.p13 chr19: 50,842,626-50,844,481 NAPSB, LOC105372437
    nsv5021035copy number variation1nstd200human GRCh38 chr19: 50,337,594-50,341,776 , GRCh37.p13 chr19: 50,840,851-50,845,033 LOC105372437, NAPSB
    nsv5021034copy number variation1nstd200human GRCh38 chr19: 50,331,919-50,336,816 , GRCh37.p13 chr19: 50,835,176-50,840,073 NAPSB, KCNC3, 1 more genes
    nsv4853373copy number variation1nstd200human GRCh37 chr19: 50,842,625-50,844,481 , GRCh38.p12 chr19: 50,339,368-50,341,224 NAPSB, LOC105372437
    nsv4853372copy number variation1nstd200human GRCh37 chr19: 50,840,641-50,865,219 , GRCh38.p12 chr19: 50,337,384-50,361,962 LOC105372437, NAPSA, 1 more genes
    nsv4853371copy number variation1nstd200human GRCh37 chr19: 50,840,851-50,845,033 , GRCh38.p12 chr19: 50,337,594-50,341,776 NAPSB, LOC105372437
    nsv4729755copy number variation1nstd102humanPathogenic GRCh37 chr19: 48,463,931-57,095,254 , GRCh38.p12 chr19: 47,960,674-56,583,886 SIGLEC5, MED25, 574 more genes
    nsv4685764copy number variation1nstd102humannot provided GRCh37 chr19: 47,939,842-54,626,871 , GRCh38.p12 chr19: 47,436,585-54,071,460 SNAR-G1, IRF3, 453 more genes
    nsv4676357copy number variation1nstd102humanPathogenic GRCh37 chr19: 44,738,088-53,621,561 , GRCh38.p12 chr19: 44,233,935-53,118,308 MIR4324, KLK9, 485 more genes
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