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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098925copy number variation1nstd102humanPathogenic GRCh38 chr19: 15,014,099-16,261,691 , GRCh37.p13 chr19: 15,124,911-16,372,502 CYP4F12, OR1AB1P, 52 more genes
    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
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    nsv6523177copy number variation1nstd223human GRCh38 chr19: 15,352,175-15,352,666 , GRCh37.p13 chr19: 15,462,986-15,463,477 AKAP8
    nsv6314004copy number variation1nstd102humanUncertain significance GRCh37 chr19: 15,184,922-15,582,812 , GRCh38.p12 chr19: 15,074,111-15,472,001 RNU6-782P, OR10B1P, 13 more genes
    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
    nsv6056227copy number variation1nstd212human GRCh38 chr19: 15,363,303-15,363,610 , GRCh37.p13 chr19: 15,474,114-15,474,421 AKAP8
    nsv6050721copy number variation1nstd212human GRCh38 chr19: 15,362,874-15,362,952 , GRCh37.p13 chr19: 15,473,685-15,473,763 AKAP8
    nsv5977846insertion1nstd209human GRCh38 chr19: 15,353,337-15,353,337 , GRCh37.p13 chr19: 15,464,148-15,464,148 AKAP8
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5971495insertion1nstd209human GRCh38 chr19: 15,364,085-15,364,085 , GRCh37.p13 chr19: 15,474,896-15,474,896 AKAP8
    nsv5935449copy number variation1nstd209human GRCh38 chr19: 15,359,614-15,359,896 , GRCh37.p13 chr19: 15,470,425-15,470,707 AKAP8
    nsv5698213mobile element insertion1nstd211human GRCh38 chr19: 15,366,154-15,366,154 , GRCh37.p13 chr19: 15,476,965-15,476,965 AKAP8
    nsv5327809copy number variation1nstd204human GRCh38.p13 chr19: 15,375,421-15,377,979 , GRCh37.p13 chr19: 15,486,232-15,488,790 AKAP8
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