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Items: 1 to 20 of 153

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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
    nsv5531328copy number variation1nstd206human GRCh38 chr19: 19,045,667-19,046,281 , GRCh37.p13 chr19: 19,156,476-19,157,090 ARMC6
    nsv5299782copy number variation1nstd204human GRCh38.p13 chr19: 18,706,301-19,688,800 , GRCh37.p13 chr19: 18,817,111-19,799,609 , HOMER3-AS1, 37 more genes
    nsv5189550mobile element insertion1nstd203human GRCh38 chr19: 19,047,395-19,047,413 , GRCh37.p13 chr19: 19,158,204-19,158,222 ARMC6
    nsv5172411mobile element insertion1nstd203human GRCh38 chr19: 19,058,627-19,058,642 , GRCh37.p13 chr19: 19,169,436-19,169,451 ARMC6
    nsv5171003mobile element insertion1nstd203human GRCh38 chr19: 19,045,493-19,045,504 , GRCh37.p13 chr19: 19,156,302-19,156,313 ARMC6
    nsv5041043inversion1nstd200human GRCh38 chr19: 11,963,569-20,150,886 , GRCh37.p13 chr19: 12,074,384-20,193,556 , USE1, 369 more genes
    nsv5014658copy number variation1nstd200human GRCh38 chr19: 19,058,636-19,071,701 , GRCh37.p13 chr19: 19,169,445-19,182,510 ARMC6, SLC25A42
    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
    nsv4631266copy number variation1nstd183human GRCh37 chr19: 19,144,446-19,144,849 , GRCh38.p12 chr19: 19,033,637-19,034,040 ARMC6, SUGP2
    nsv4626212copy number variation1nstd183human GRCh37 chr19: 19,144,401-19,144,609 , GRCh38.p12 chr19: 19,033,592-19,033,800 SUGP2, ARMC6
    nsv4252492copy number variation1nstd166human GRCh37.p13 chr19: 19,169,456-19,182,475 , GRCh38.p12 chr19: 19,058,647-19,071,666 SLC25A42, ARMC6
    nsv3955798insertion1nstd168human GRCh38 chr19: 19,022,554-19,059,022 , GRCh37.p13 chr19: 19,133,363-19,169,831 ARMC6, SUGP2
    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
    nsv3906931copy number variation1nstd102humanBenign GRCh37 chr19: 19,168,732-19,174,922 , GRCh38.p12 chr19: 19,057,923-19,064,113 SLC25A42, ARMC6
    nsv3904885copy number variation1nstd102humanPathogenic GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923 ZNF321P, ZNF861P, 2443 more genes
    nsv3903203copy number variation1nstd102humanPathogenic GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793 BABAM1, BEST2, 2426 more genes
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