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Items: 1 to 20 of 135

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095477copy number variation1nstd102humanUncertain significance GRCh37 chr19: 17,927,663-19,312,528 , GRCh38.p12 chr19: 17,816,854-19,201,719 BORCS8, ARMC6, 60 more genes
    nsv7095198copy number variation1nstd102humanPathogenic GRCh37 chr19: 18,709,222-18,710,676 , GRCh38.p12 chr19: 18,598,412-18,599,866 CRLF1
    nsv7065580inversion1nstd229human GRCh38 chr19: 11,963,576-20,150,892 , GRCh37.p13 chr19: 12,074,391-20,193,556 CYP4F24P, CYP4F2, 359 more genes
    nsv7063889inversion1nstd229human GRCh38 chr19: 17,856,052-19,078,279 , GRCh37.p13 chr19: 17,966,861-19,189,088 REX1BD, CRLF1, 52 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
    nsv6532233copy number variation1nstd223human GRCh38 chr19: 18,602,946-18,609,058 , GRCh37.p13 chr19: 18,713,756-18,719,868 CRLF1
    nsv6521635copy number variation1nstd223human GRCh38 chr19: 17,313,484-18,689,472 , GRCh37.p13 chr19: 17,424,293-18,800,282 NIBAN3, CRTC1, 64 more genes
    nsv6284954copy number variation1nstd214human GRCh38 chr19: 18,600,229-18,600,398 , GRCh37.p13 chr19: 18,711,039-18,711,208 CRLF1
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5931491copy number variation1nstd209human GRCh38 chr19: 18,591,378-18,591,690 , GRCh37.p13 chr19: 18,702,188-18,702,500 CRLF1, REX1BD
    nsv5713798mobile element insertion2nstd211human GRCh38 chr19: 18,595,748-18,595,748 , GRCh37.p13 chr19: 18,706,558-18,706,558 CRLF1
    nsv5422722mobile element insertion1nstd206human GRCh38 chr19: 18,595,748-18,595,799 , GRCh37.p13 chr19: 18,706,558-18,706,609 CRLF1
    nsv5359556translocation1nstd200human GRCh38 chr19: 18,600,971-18,600,971 , GRCh38 chr19: 18,601,052-18,601,052 , GRCh37.p13 chr19: 18,711,781-18,711,781 , GRCh37.p13 chr19: 18,711,862-18,711,862 CRLF1
    nsv5289668copy number variation1nstd204human GRCh37.p13 chr19: 18,552,711-18,764,410 , GRCh38.p13 chr19: 18,441,901-18,653,600 UBA52, ELL, 7 more genes
    nsv5282384copy number variation1nstd204human GRCh38.p13 chr19: 18,292,801-18,706,100 , GRCh37.p13 chr19: 18,403,611-18,816,910 ELL, FKBP8, 17 more genes
    nsv5167123mobile element insertion1nstd203human GRCh38 chr19: 18,597,431-18,597,447 , GRCh37.p13 chr19: 18,708,241-18,708,257 CRLF1
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5019431copy number variation1nstd200human GRCh38 chr19: 18,601,915-18,602,923 , GRCh37.p13 chr19: 18,712,725-18,713,733 CRLF1
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