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Items: 1 to 20 of 109

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv7058723inversion1nstd229human GRCh38 chr19: 13,672,973-14,832,292 , GRCh37.p13 chr19: 13,783,787-14,943,104 SNRPGP15, NDUFB7, 53 more genes
    nsv7009275copy number variation1nstd229human GRCh38 chr19: 13,836,899-14,088,244 , GRCh37.p13 chr19: 13,947,713-14,199,056 NANOS3, RLN3, 17 more genes
    nsv7005996copy number variation1nstd229human GRCh38 chr19: 13,725,201-13,895,200 , GRCh37.p13 chr19: 13,836,015-14,006,013 NANOS3, MIR23AHG, 12 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
    nsv6528334copy number variation1nstd223human GRCh38 chr19: 13,827,510-13,835,108 , GRCh37.p13 chr19: 13,938,324-13,945,922 MIR27A, MIR23AHG, 3 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
    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
    nsv5300223copy number variation1nstd204human GRCh38.p13 chr19: 13,638,301-14,767,500 , GRCh37.p13 chr19: 13,749,115-14,878,312 , SNORA104, 53 more genes
    nsv5286173copy number variation1nstd204human GRCh38.p13 chr19: 13,764,801-14,012,000 , GRCh37.p13 chr19: 13,875,615-14,122,812 , MIR181C, 16 more genes
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv4632244copy number variation2nstd183human GRCh37 chr19: 13,947,125-13,947,309 , GRCh38.p12 chr19: 13,836,311-13,836,495 MIR27A, MIR23AHG, 2 more genes
    nsv4258130copy number variation1nstd166human GRCh37.p13 chr19: 13,937,414-13,946,296 , GRCh38.p12 chr19: 13,826,600-13,835,482 ZSWIM4, MIR27A, 3 more genes
    nsv3924466copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,496,978-14,126,833 , GRCh38 chr19: 11,525,163-14,155,021 , GRCh37 chr19: 11,635,978-14,265,833 JUNB, ZNF442, 135 more genes
    nsv3923415copy number variation1nstd102humanPathogenic NCBI36 chr19: 10,286,934-14,020,806 , GRCh37 chr19: 10,425,934-14,159,806 , GRCh38 chr19: 10,315,258-14,048,994 MAN2B1, SWSAP1, 182 more genes
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