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Items: 1 to 20 of 116

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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
    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
    nsv7002469copy number variation1nstd229human GRCh38 chr19: 18,618,037-18,632,331 , GRCh37.p13 chr19: 18,728,847-18,743,141 RN7SL155P, TMEM59L
    nsv7000144copy number variation1nstd229human GRCh38 chr19: 18,613,507-18,618,477 , GRCh37.p13 chr19: 18,724,317-18,729,287 TMEM59L
    nsv6599077inversion1nstd223human GRCh38 chr19: 12,342,953-19,691,233 , GRCh37.p13 chr19: 12,453,767-19,802,042 GET3, BST2, 314 more genes
    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
    nsv6133400copy number variation1nstd213human GRCh37 chr19: 18,720,000-20,740,001 , GRCh38.p12 chr19: 18,609,190-20,557,195 COMP, NCAN, 81 more genes
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    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
    nsv5194433mobile element insertion1nstd203human GRCh38 chr19: 18,612,368-18,612,384 , GRCh37.p13 chr19: 18,723,178-18,723,194 TMEM59L
    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
    nsv3922457copy number variation1nstd102humanPathogenic GRCh37 chr19: 14,085,489-28,330,584 , GRCh38 chr19: 13,974,677-27,839,676 , NCBI36 chr19: 13,946,489-33,022,424 REX1BD, ZNF92P2, 416 more genes
    nsv3921076copy number variation1nstd102humanPathogenic GRCh38 chr19: 15,133,594-24,193,591 , GRCh37 chr19: 15,244,405-24,376,393 , NCBI36 chr19: 15,105,405-24,168,233 MRPL34, BNIP3P25, 358 more genes
    nsv3914228copy number variation1nstd102humanPathogenic NCBI36 chr19: 17,148,576-40,106,894 , GRCh38 chr19: 17,176,767-34,924,150 , GRCh37 chr19: 17,287,576-35,415,054 LOC105372355, SUGP2, 411 more genes
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
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