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Items: 1 to 20 of 101

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5930276copy number variation1nstd209human GRCh38 chr19: 21,439,885-21,545,621 , GRCh37.p13 chr19: 21,622,687-21,728,423 ZNF429, LINC00664, 2 more genes
    nsv5885841copy number variation1nstd209human GRCh38 chr19: 21,515,909-21,520,408 , GRCh37.p13 chr19: 21,698,711-21,703,210 ZNF429, BNIP3P26
    nsv5391587copy number variation1nstd186human GRCh37 chr19: 21,682,826-21,778,292 , GRCh38.p12 chr19: 21,500,024-21,595,490 ZNF429, LINC00664, 3 more genes
    nsv5389832copy number variation1nstd186human GRCh37 chr19: 21,682,753-21,778,292 , GRCh38.p12 chr19: 21,499,951-21,595,490 ZNF429, LINC00664, 3 more genes
    nsv5329381copy number variation1nstd204human GRCh38.p13 chr19: 21,499,413-21,596,037 , GRCh37.p13 chr19: 21,682,215-21,778,839 LINC00664, BNIP3P26, 3 more genes
    nsv5014727copy number variation1nstd200human GRCh38 chr19: 21,499,882-21,595,618 , GRCh37.p13 chr19: 21,682,684-21,778,420 LINC00664, ZNF429, 3 more genes
    nsv5014722copy number variation1nstd200human GRCh38 chr19: 21,304,937-21,672,253 , GRCh37.p13 chr19: 21,487,739-21,855,055 ZNF738, LOC101929007, 10 more genes
    nsv4865035copy number variation1nstd200human GRCh37 chr19: 21,682,750-21,778,293 , GRCh38.p12 chr19: 21,499,948-21,595,491 LOC101929007, ZNF429, 3 more genes
    nsv4676395copy number variation1nstd102humanUncertain significance GRCh37 chr19: 21,683,086-21,777,328 , GRCh38.p12 chr19: 21,500,284-21,594,526 LOC101929007, ZNF429, 3 more genes
    nsv4436023complex substitution1nstd102humanUncertain significance GRCh38.p12 chr19: 19,120,059-23,932,567 , GRCh37 chr19: 19,230,868-24,115,369 NCAN, BORCS8-MEF2B, 195 more genes
    nsv4425619copy number variation1nstd174human GRCh37 chr19: 21,265,468-21,839,466 , GRCh38.p12 chr19: 21,082,662-21,656,664 LOC400682, VN1R82P, 19 more genes
    nsv4417587copy number variation1nstd174human GRCh37 chr19: 21,685,778-21,755,476 , GRCh38.p12 chr19: 21,502,976-21,572,674 ZNF429, LINC00664, 2 more genes
    nsv4263048copy number variation1nstd166human GRCh37.p13 chr19: 21,563,171-21,942,807 , GRCh38.p12 chr19: 21,380,369-21,760,005 MTDHP4, BNIP3P26, 13 more genes
    nsv3971059insertion1nstd168human GRCh38 chr19: 21,494,545-21,737,804 , GRCh37.p13 chr19: 21,677,347-21,920,606 ZNF100, MTDHP3, 8 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
    nsv3918940copy number variation1nstd102humanUncertain significance GRCh37 chr19: 20,820,793-22,159,018 , GRCh38 chr19: 20,637,987-21,976,216 , NCBI36 chr19: 20,612,633-21,950,858 LOC100418988, LOC100418991, 51 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
    nsv3907631copy number variation1nstd102humanUncertain significance GRCh37 chr19: 19,903,805-21,966,609 , GRCh38.p12 chr19: 19,792,996-21,783,807 ZNF431, ISCA1P5, 84 more genes
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