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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974799inversion1nstd209human GRCh38 chr19: 12,342,936-19,691,231 , GRCh37.p13 chr19: 12,453,750-19,802,040 , GET3, 322 more genes
    nsv5944859copy number variation1nstd209human GRCh38 chr19: 17,437,864-17,437,941 , GRCh37.p13 chr19: 17,548,673-17,548,750 TMEM221
    nsv5299651copy number variation1nstd204human GRCh38.p13 chr19: 16,996,101-18,292,600 , GRCh37.p13 chr19: 17,106,911-18,403,410 ANO8, MPV17L2, 57 more genes
    nsv5286520copy number variation1nstd204human GRCh38.p13 chr19: 17,091,201-17,638,100 , GRCh37.p13 chr19: 17,202,011-17,748,909 PGLS, LOC105372298, 27 more genes
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5019377copy number variation1nstd200human GRCh38 chr19: 17,448,244-17,451,933 , GRCh37.p13 chr19: 17,559,053-17,562,742 TMEM221
    nsv4860571copy number variation1nstd200human GRCh37 chr19: 17,559,053-17,562,742 , GRCh38.p12 chr19: 17,448,244-17,451,933 TMEM221
    nsv4860570copy number variation1nstd200human GRCh37 chr19: 17,550,268-17,550,739 , GRCh38.p12 chr19: 17,439,459-17,439,930 TMEM221
    nsv4860569copy number variation1nstd200human GRCh37 chr19: 17,544,604-17,546,817 , GRCh38.p12 chr19: 17,433,795-17,436,008 TMEM221
    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
    nsv4258307copy number variation1nstd166human GRCh37.p13 chr19: 17,548,680-17,548,751 , GRCh38.p12 chr19: 17,437,871-17,437,942 TMEM221
    nsv4257363copy number variation1nstd166human GRCh37.p13 chr19: 17,559,053-17,562,742 , GRCh38.p12 chr19: 17,448,244-17,451,933 TMEM221
    nsv3931206insertion1nstd167human GRCh37 chr19: 17,555,519-17,555,519 , GRCh38.p12 chr19: 17,444,710-17,444,710 TMEM221
    nsv3923633copy number variation1nstd102humanUncertain significance GRCh38 chr19: 17,246,895-17,730,147 , GRCh37 chr19: 17,357,704-17,840,956 , NCBI36 chr19: 17,218,704-17,701,956 ANKLE1, MRPL34, 23 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
    nsv3915960copy number variation1nstd102humanUncertain significance GRCh37 chr19: 17,419,016-17,816,191 , GRCh38 chr19: 17,308,207-17,705,382 , NCBI36 chr19: 17,280,016-17,677,191 NXNL1, BST2, 17 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
    nsv3905183copy number variation1nstd102humanUncertain significance GRCh37 chr19: 17,325,373-17,840,956 , GRCh38.p12 chr19: 17,214,564-17,730,147 ABHD8, MAP1S, 26 more genes
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