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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095640copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 13,136,156-13,151,380 , GRCh38.p12 chr19: 13,025,342-13,040,566 NFIX
    nsv7095639copy number variation2nstd102humanUncertain significance GRCh37 chr19: 13,135,448-13,419,362 , GRCh38.p12 chr19: 13,024,634-13,308,548 IER2, RPL12P42, 7 more genes
    nsv7095458copy number variation4nstd102humanUncertain significance GRCh37 chr19: 10,828,919-13,482,613 , GRCh38.p12 chr19: 10,718,243-13,371,799 WDR83OS, RPL10P16, 140 more genes
    nsv7095400copy number variation1nstd102humanUncertain significance GRCh37 chr19: 11,277,234-13,249,220 , GRCh38.p12 chr19: 11,166,558-13,138,406 ZNF627, RGL3, 120 more genes
    nsv7075473inversion1nstd229human GRCh38 chr19: 12,694,752-17,614,167 , GRCh37.p13 chr19: 12,805,566-17,724,976 SYDE1, LOC107985287, 207 more genes
    nsv7065580inversion1nstd229human GRCh38 chr19: 11,963,576-20,150,892 , GRCh37.p13 chr19: 12,074,391-20,193,556 CYP4F24P, CYP4F2, 359 more genes
    nsv7063135inversion1nstd229human GRCh38 chr19: 12,625,698-17,530,884 , GRCh37.p13 chr19: 12,736,512-17,641,693 SYCE2, OR1AB1P, 212 more genes
    nsv7060542inversion1nstd229human GRCh38 chr19: 12,342,956-19,691,233 , GRCh37.p13 chr19: 12,453,770-19,802,042 DDX39A, KCNN1, 314 more genes
    nsv7059139inversion1nstd229human GRCh38 chr19: 12,641,624-19,910,103 , GRCh37.p13 chr19: 12,752,438-20,020,912 NR2F6, ISCA1P5, 307 more genes
    nsv7014038copy number variation1nstd229human GRCh38 chr19: 13,037,030-13,037,502 , GRCh37.p13 chr19: 13,147,844-13,148,316 NFIX
    nsv7013718copy number variation1nstd229human GRCh38 chr19: 13,033,637-13,033,856 , GRCh37.p13 chr19: 13,144,451-13,144,670 NFIX
    nsv7009597copy number variation1nstd229human GRCh38 chr19: 13,038,252-13,040,840 , GRCh37.p13 chr19: 13,149,066-13,151,654 NFIX
    nsv7009567copy number variation1nstd229human GRCh38 chr19: 13,092,081-13,092,759 , GRCh37.p13 chr19: 13,202,895-13,203,573 NFIX
    nsv7003988copy number variation1nstd229human GRCh38 chr19: 13,043,710-13,048,273 , GRCh37.p13 chr19: 13,154,524-13,159,087 NFIX
    nsv7000534copy number variation1nstd229human GRCh38 chr19: 13,090,390-13,094,630 , GRCh37.p13 chr19: 13,201,204-13,205,444 NFIX
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6598197inversion1nstd223human GRCh38 chr19: 13,041,493-13,042,243 , GRCh37.p13 chr19: 13,152,307-13,153,057 NFIX
    nsv6523555copy number variation1nstd223human GRCh38 chr19: 13,096,601-13,097,300 , GRCh37.p13 chr19: 13,207,415-13,208,114 NFIX, LYL1
    nsv6522825copy number variation1nstd223human GRCh38 chr19: 13,037,030-13,037,507 , GRCh37.p13 chr19: 13,147,844-13,148,321 NFIX
    nsv6314597complex chromosomal rearrangement2nstd102humanPathogenic GRCh38.p12 chr19: 13,020,711-13,020,711 , GRCh38.p12 chr19: 13,023,836-13,023,836 , GRCh37 chr19: 13,131,525-13,131,525 , GRCh37 chr19: 13,134,650-13,134,650 , GRCh37 chr5: 162,651,347-162,651,347 , GRCh37 chr5: 162,659,654-162,659,654 , GRCh38.p12 chr5: 163,224,341-163,224,341 , GRCh38.p12 chr5: 163,232,648-163,232,648 NFIX, LOC105377700
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