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Items: 1 to 20 of 128

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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
    nsv7005340copy number variation1nstd229human GRCh38 chr19: 16,323,291-16,323,371 , GRCh37.p13 chr19: 16,434,102-16,434,182 KLF2
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6242818mobile element insertion1nstd215human GRCh38 chr19: 16,327,487-16,327,487 , GRCh37.p13 chr19: 16,438,298-16,438,298 KLF2
    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
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5928821copy number variation1nstd209human GRCh38 chr19: 16,314,497-16,331,261 , GRCh37.p13 chr19: 16,425,308-16,442,072 KLF2
    nsv5880747copy number variation1nstd209human GRCh38 chr19: 16,314,493-16,324,436 , GRCh37.p13 chr19: 16,425,304-16,435,247 KLF2
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    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
    nsv4624487copy number variation1nstd183human GRCh37 chr19: 16,435,685-16,438,838 , GRCh38.p12 chr19: 16,324,874-16,328,027 KLF2
    nsv4503842mobile element insertion1nstd166human GRCh37.p13 chr19: 16,438,553-16,438,553 , GRCh38.p12 chr19: 16,327,742-16,327,742 KLF2
    nsv4272282copy number variation1nstd166human GRCh37.p13 chr19: 16,434,975-16,440,000 , GRCh38.p12 chr19: 16,324,164-16,329,189 KLF2
    nsv4253783copy number variation1nstd166human GRCh37.p13 chr19: 16,436,986-16,437,077 , GRCh38.p12 chr19: 16,326,175-16,326,266 KLF2
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