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Items: 1 to 20 of 562

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095645copy number variation1nstd102humanUncertain significance GRCh37 chr19: 14,847,048-17,394,124 , GRCh38.p12 chr19: 14,736,236-17,283,315 HAUS8, MIR1470, 95 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
    nsv7017462copy number variation1nstd229human GRCh38 chr19: 16,952,625-16,953,221 , GRCh37.p13 chr19: 17,063,435-17,064,031 CPAMD8
    nsv7014829copy number variation1nstd229human GRCh38 chr19: 16,907,497-16,908,043 , GRCh37.p13 chr19: 17,018,307-17,018,853 RN7SL835P, CPAMD8
    nsv7014718copy number variation1nstd229human GRCh38 chr19: 16,907,496-16,908,165 , GRCh37.p13 chr19: 17,018,306-17,018,975 RN7SL835P, CPAMD8
    nsv7013462copy number variation1nstd229human GRCh38 chr19: 16,978,092-16,984,574 , GRCh37.p13 chr19: 17,088,902-17,095,384 CPAMD8
    nsv7011394copy number variation1nstd229human GRCh38 chr19: 16,965,924-16,969,934 , GRCh37.p13 chr19: 17,076,734-17,080,744 CPAMD8
    nsv7010583copy number variation1nstd229human GRCh38 chr19: 16,936,001-16,939,100 , GRCh37.p13 chr19: 17,046,811-17,049,910 CPAMD8
    nsv7010284copy number variation1nstd229human GRCh38 chr19: 16,943,144-16,952,455 , GRCh37.p13 chr19: 17,053,954-17,063,265 CPAMD8
    nsv7009028copy number variation1nstd229human GRCh38 chr19: 17,021,739-17,029,071 , GRCh37.p13 chr19: 17,132,549-17,139,881 CPAMD8
    nsv7008384copy number variation1nstd229human GRCh38 chr19: 17,004,557-17,010,760 , GRCh37.p13 chr19: 17,115,367-17,121,570 CPAMD8
    nsv7008306copy number variation1nstd229human GRCh38 chr19: 16,997,625-16,997,663 , GRCh37.p13 chr19: 17,108,435-17,108,473 CPAMD8
    nsv7007560copy number variation1nstd229human GRCh38 chr19: 16,976,333-16,976,834 , GRCh37.p13 chr19: 17,087,143-17,087,644 CPAMD8
    nsv7006942copy number variation1nstd229human GRCh38 chr19: 16,900,968-16,909,718 , GRCh37.p13 chr19: 17,011,779-17,020,528 RN7SL835P, CPAMD8, 1 more genes
    nsv7005471copy number variation1nstd229human GRCh38 chr19: 17,006,893-17,006,928 , GRCh37.p13 chr19: 17,117,703-17,117,738 CPAMD8
    nsv7005060copy number variation1nstd229human GRCh38 chr19: 16,961,010-16,965,449 , GRCh37.p13 chr19: 17,071,820-17,076,259 CPAMD8
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