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Items: 1 to 20 of 123

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7141847copy number variation1nstd232human GRCh37.p13 chr19: 16,631,076-16,631,173 , GRCh38.p12 chr19: 16,520,265-16,520,362 CHERP, C19orf44
    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
    nsv7017852copy number variation1nstd229human GRCh38 chr19: 16,511,292-16,516,056 , GRCh37.p13 chr19: 16,622,103-16,626,867 C19orf44, CHERP
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6522578copy number variation1nstd223human GRCh38 chr19: 16,538,576-16,539,365 , GRCh37.p13 chr19: 16,649,387-16,650,176 RN7SL146P, CHERP
    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
    nsv6133690copy number variation1nstd213human GRCh37 chr19: 13,260,000-16,840,001 , GRCh38.p12 chr19: 13,149,186-16,729,190 PRKACA, SLC1A6, 137 more genes
    nsv6059264copy number variation1nstd212human GRCh38 chr19: 16,538,507-16,538,580 , GRCh37.p13 chr19: 16,649,318-16,649,391 RN7SL146P, CHERP
    nsv6044111copy number variation1nstd212human GRCh38 chr19: 16,540,632-16,540,957 , GRCh37.p13 chr19: 16,651,443-16,651,768 CHERP
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5520999copy number variation1nstd206human GRCh38 chr19: 16,526,702-16,526,960 , GRCh37.p13 chr19: 16,637,513-16,637,771 CHERP
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv4860520copy number variation1nstd200human GRCh37 chr19: 16,624,583-16,626,730 , GRCh38.p12 chr19: 16,513,772-16,515,919 CHERP, C19orf44
    nsv4733475copy number variation1nstd199human GRCh37 chr19: 16,649,215-16,649,400 , GRCh38.p12 chr19: 16,538,404-16,538,589 CHERP, RN7SL146P
    nsv4729750copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,286,624-20,956,753 , GRCh38.p12 chr19: 14,175,812-20,773,947 LOC105372309, RAB8A, 269 more genes
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