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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139231insertion1nstd232human GRCh37.p13 chr19: 33,526,726-33,526,726 , GRCh38.p12 chr19: 33,035,820-33,035,820 RHPN2
    nsv7095478copy number variation1nstd102humanUncertain significance GRCh37 chr19: 33,167,170-36,643,309 , GRCh38.p12 chr19: 32,676,264-36,152,407 NFKBID, LRP3, 141 more genes
    nsv7064982inversion1nstd229human GRCh38 chr19: 32,032,146-33,117,941 , GRCh37.p13 chr19: 32,523,052-33,608,847 LINC01782, NUDT19, 22 more genes
    nsv7016316copy number variation1nstd229human GRCh38 chr19: 33,062,190-33,069,257 , GRCh37.p13 chr19: 33,553,096-33,560,163 RHPN2
    nsv7013254copy number variation1nstd229human GRCh38 chr19: 33,009,635-33,010,837 , GRCh37.p13 chr19: 33,500,541-33,501,743 RHPN2
    nsv7011083copy number variation1nstd229human GRCh38 chr19: 33,056,901-33,062,800 , GRCh37.p13 chr19: 33,547,807-33,553,706 RHPN2
    nsv7010919copy number variation1nstd229human GRCh38 chr19: 32,988,617-32,988,649 , GRCh37.p13 chr19: 33,479,523-33,479,555 RHPN2
    nsv7005903copy number variation1nstd229human GRCh38 chr19: 32,703,671-33,040,255 , GRCh37.p13 chr19: 33,194,577-33,531,161 SLC7A9, NUDT19, 7 more genes
    nsv7005548copy number variation1nstd229human GRCh38 chr19: 32,976,101-32,983,100 , GRCh37.p13 chr19: 33,467,007-33,474,006 RHPN2, FAAP24
    nsv7004683copy number variation1nstd229human GRCh38 chr19: 32,931,662-33,016,377 , GRCh37.p13 chr19: 33,422,568-33,507,283 RPL31P60, FAAP24, 2 more genes
    nsv7001430copy number variation1nstd229human GRCh38 chr19: 33,034,578-33,045,476 , GRCh37.p13 chr19: 33,525,484-33,536,382 RHPN2
    nsv7000122copy number variation1nstd229human GRCh38 chr19: 33,002,101-33,005,800 , GRCh37.p13 chr19: 33,493,007-33,496,706 RHPN2
    nsv6599716inversion1nstd223human GRCh38 chr19: 33,038,126-33,038,913 , GRCh37.p13 chr19: 33,529,032-33,529,819 RHPN2
    nsv6599462inversion1nstd223human GRCh38 chr19: 33,044,908-33,045,290 , GRCh37.p13 chr19: 33,535,814-33,536,196 RHPN2
    nsv6599330inversion1nstd223human GRCh38 chr19: 32,989,166-32,990,122 , GRCh37.p13 chr19: 33,480,072-33,481,028 RHPN2
    nsv6598652inversion1nstd223human GRCh38 chr19: 33,019,582-33,020,503 , GRCh37.p13 chr19: 33,510,488-33,511,409 RHPN2
    nsv6597479inversion1nstd223human GRCh38 chr19: 32,994,951-32,995,115 , GRCh37.p13 chr19: 33,485,857-33,486,021 RHPN2
    nsv6596670inversion1nstd223human GRCh38 chr19: 32,032,144-33,117,460 , GRCh37.p13 chr19: 32,523,050-33,608,366 DPY19L3, LINC01782, 22 more genes
    nsv6532686copy number variation1nstd223human GRCh38 chr19: 33,045,730-33,048,312 , GRCh37.p13 chr19: 33,536,636-33,539,218 RHPN2
    nsv6532513copy number variation1nstd223human GRCh38 chr19: 33,032,721-33,036,500 , GRCh37.p13 chr19: 33,523,627-33,527,406 RHPN2
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