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Items: 1 to 20 of 196

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979386insertion1nstd209human GRCh38 chr17: 65,037,777-65,037,777 , GRCh37.p13 chr17: 63,033,895-63,033,895 GNA13
    nsv5711916mobile element insertion2nstd211human GRCh38 chr17: 65,048,331-65,048,331 , GRCh37.p13 chr17: 63,044,449-63,044,449 GNA13
    nsv5698091mobile element insertion1nstd211human GRCh38 chr17: 65,037,800-65,037,800 , GRCh37.p13 chr17: 63,033,918-63,033,918 GNA13
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5423230mobile element insertion1nstd206human GRCh38 chr17: 65,048,331-65,048,382 , GRCh37.p13 chr17: 63,044,449-63,044,500 GNA13
    nsv5359022translocation1nstd200human GRCh38 chr17: 65,037,529-65,037,529 , GRCh38 chr17: 65,036,682-65,036,682 , GRCh37.p13 chr17: 63,033,647-63,033,647 , GRCh37.p13 chr17: 63,032,800-63,032,800 GNA13
    nsv5190012mobile element insertion1nstd203human GRCh38 chr17: 65,023,361-65,023,369 , GRCh37.p13 chr17: 63,019,479-63,019,487 GNA13
    nsv5158481mobile element insertion1nstd203human GRCh38 chr17: 65,048,321-65,048,331 , GRCh37.p13 chr17: 63,044,439-63,044,449 GNA13
    nsv5158298mobile element insertion1nstd203human GRCh38 chr17: 65,018,091-65,018,139 , GRCh37.p13 chr17: 63,014,209-63,014,257 GNA13
    nsv5157372mobile element insertion1nstd203human GRCh38 chr17: 65,018,093-65,018,131 , GRCh37.p13 chr17: 63,014,211-63,014,249 GNA13
    nsv5156035mobile element insertion1nstd203human GRCh38 chr17: 65,018,113-65,018,139 , GRCh37.p13 chr17: 63,014,231-63,014,257 GNA13
    nsv5155198mobile element insertion1nstd203human GRCh38 chr17: 65,045,042-65,045,083 , GRCh37.p13 chr17: 63,041,160-63,041,201 GNA13
    nsv5148505mobile element insertion1nstd203human GRCh38 chr17: 65,018,096-65,018,139 , GRCh37.p13 chr17: 63,014,214-63,014,257 GNA13
    nsv5144056mobile element insertion1nstd203human GRCh38 chr17: 65,018,095-65,018,136 , GRCh37.p13 chr17: 63,014,213-63,014,254 GNA13
    nsv5141879mobile element insertion1nstd203human GRCh38 chr17: 65,018,092-65,018,139 , GRCh37.p13 chr17: 63,014,210-63,014,257 GNA13
    nsv5029562inversion1nstd200human GRCh38 chr17: 64,441,870-75,217,767 , GRCh37.p13 chr17: 62,649,312-73,213,862 , LOC102929163, 207 more genes
    nsv5013936copy number variation1nstd200human GRCh38 chr17: 65,037,720-65,038,211 , GRCh37.p13 chr17: 63,033,838-63,034,329 GNA13
    nsv4577533mobile element insertion1nstd166human GRCh37.p13 chr17: 63,049,517-63,049,517 , GRCh38.p12 chr17: 65,053,399-65,053,399 GNA13
    nsv4505545mobile element insertion1nstd166human GRCh37.p13 chr17: 63,044,439-63,044,439 , GRCh38.p12 chr17: 65,048,321-65,048,321 GNA13
    nsv4457799copy number variation1nstd102humanPathogenic GRCh37 chr17: 57,869,604-67,078,443 , GRCh38.p12 chr17: 59,792,243-69,082,302 PECAM1, TBX2-AS1, 215 more genes
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