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Items: 1 to 20 of 140

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7144998insertion1nstd232human GRCh37.p13 chr19: 13,058,823-13,058,823 , GRCh38.p12 chr19: 12,948,009-12,948,009 RAD23A
    nsv7137366copy number variation1nstd232human GRCh37.p13 chr19: 13,063,666-13,063,747 , GRCh38.p12 chr19: 12,952,852-12,952,933 RAD23A, GADD45GIP1
    nsv7095458copy number variation4nstd102humanUncertain significance GRCh37 chr19: 10,828,919-13,482,613 , GRCh38.p12 chr19: 10,718,243-13,371,799 WDR83OS, RPL10P16, 140 more genes
    nsv7095400copy number variation1nstd102humanUncertain significance GRCh37 chr19: 11,277,234-13,249,220 , GRCh38.p12 chr19: 11,166,558-13,138,406 ZNF627, RGL3, 120 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
    nsv7015563copy number variation1nstd229human GRCh38 chr19: 12,943,501-12,949,400 , GRCh37.p13 chr19: 13,054,315-13,060,214 CALR, RAD23A
    nsv7014063copy number variation1nstd229human GRCh38 chr19: 12,949,408-12,952,685 , GRCh37.p13 chr19: 13,060,222-13,063,499 GADD45GIP1, RAD23A
    nsv7005114copy number variation1nstd229human GRCh38 chr19: 12,938,693-12,964,357 , GRCh37.p13 chr19: 13,049,507-13,075,171 RAD23A, GADD45GIP1, 2 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
    nsv6310464copy number variation1nstd102humanUncertain significance GRCh37 chr19: 12,917,488-13,205,463 , GRCh38.p12 chr19: 12,806,674-13,094,649 LOC105372281, SYCE2, 18 more genes
    nsv6310462copy number variation2nstd102humanPathogenic GRCh37 chr19: 12,757,434-13,617,038 , GRCh38.p12 chr19: 12,646,620-13,506,224 DHPS, JUNB, 42 more genes
    nsv6291633copy number variation1nstd102humanPathogenic GRCh37 chr19: 12,697,728-14,111,313 , GRCh38.p12 chr19: 12,586,914-14,000,501 RN7SL619P, MIR6515, 67 more genes
    nsv6133689copy number variation1nstd213human GRCh37 chr19: 11,220,000-13,700,001 , GRCh38.p12 chr19: 11,109,324-13,589,187 ACP5, GET3, 128 more genes
    nsv6133687copy number variation1nstd213human GRCh37 chr19: 13,046,032-13,117,737 , GRCh38.p12 chr19: 12,935,218-13,006,923 CALR, NFIX, 4 more genes
    nsv6133479copy number variation1nstd213human GRCh37 chr19: 7,400,000-13,280,001 , GRCh38.p12 chr19: 7,335,095-13,169,187 , ACP5, 299 more genes
    nsv6133465copy number variation1nstd213human GRCh37 chr19: 13,046,044-13,117,742 , GRCh38.p12 chr19: 12,935,230-13,006,928 CALR, NFIX, 4 more genes
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