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Items: 1 to 20 of 191

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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
    nsv7015282copy number variation1nstd229human GRCh38 chr19: 16,824,187-16,828,689 , GRCh37.p13 chr19: 16,934,998-16,939,500 SIN3B
    nsv7004911copy number variation1nstd229human GRCh38 chr19: 16,817,573-17,564,195 , GRCh37.p13 chr19: 16,928,384-17,675,004 BISPR, NWD1, 32 more genes
    nsv7001645copy number variation1nstd229human GRCh38 chr19: 16,869,171-16,869,332 , GRCh37.p13 chr19: 16,979,982-16,980,143 SIN3B
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6529327copy number variation1nstd223human GRCh38 chr19: 16,875,557-16,875,774 , GRCh37.p13 chr19: 16,986,368-16,986,585 SIN3B
    nsv6528153copy number variation1nstd223human GRCh38 chr19: 16,861,008-16,862,213 , GRCh37.p13 chr19: 16,971,819-16,973,024 SIN3B
    nsv6515603copy number variation1nstd223human GRCh38 chr19: 16,875,158-16,875,221 , GRCh37.p13 chr19: 16,985,969-16,986,032 SIN3B
    nsv6201123copy number variation1nstd214human GRCh38 chr19: 16,853,832-16,853,897 , GRCh37.p13 chr19: 16,964,643-16,964,708 SIN3B
    nsv6189064copy number variation1nstd214human GRCh38 chr19: 16,874,386-16,874,442 , GRCh37.p13 chr19: 16,985,197-16,985,253 SIN3B
    nsv6133691copy number variation1nstd213human GRCh37 chr19: 15,360,000-18,450,001 , GRCh38.p12 chr19: 15,249,189-18,339,191 BST2, NR2F6, 123 more genes
    nsv6050153copy number variation1nstd212human GRCh38 chr19: 16,875,179-16,875,243 , GRCh37.p13 chr19: 16,985,990-16,986,054 SIN3B
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5944522copy number variation1nstd209human GRCh38 chr19: 16,832,237-16,832,539 , GRCh37.p13 chr19: 16,943,048-16,943,350 SIN3B
    nsv5941314copy number variation1nstd209human GRCh38 chr19: 16,875,741-16,875,836 , GRCh37.p13 chr19: 16,986,552-16,986,647 SIN3B
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