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Items: 1 to 20 of 674

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980461insertion1nstd102humanLikely benign GRCh37 chr10: 88,649,976-88,649,976 , GRCh38 chr10: 86,890,219-86,890,219 BMPR1A, RNU1-19P
    nsv5960726insertion1nstd209human GRCh38 chr10: 86,925,694-86,925,694 , GRCh37.p13 chr10: 88,685,451-88,685,451 BMPR1A
    nsv5955083insertion1nstd209human GRCh38 chr10: 86,824,105-86,824,105 , GRCh37.p13 chr10: 88,583,862-88,583,862 BMPR1A
    nsv5949850insertion1nstd209human GRCh38 chr10: 86,791,680-86,791,680 , GRCh37.p13 chr10: 88,551,437-88,551,437 BMPR1A
    nsv5926561copy number variation1nstd209human GRCh38 chr10: 79,825,669-87,341,680 , GRCh37.p13 chr10: 81,585,425-89,101,437 , RPL12P29, 110 more genes
    nsv5925659copy number variation1nstd209human GRCh38 chr10: 86,906,418-86,906,757 , GRCh37.p13 chr10: 88,666,175-88,666,514 BMPR1A
    nsv5924859copy number variation1nstd209human GRCh38 chr10: 86,879,043-86,879,117 , GRCh37.p13 chr10: 88,638,800-88,638,874 BMPR1A
    nsv5915318copy number variation1nstd209human GRCh38 chr10: 86,927,111-86,927,304 , GRCh37.p13 chr10: 88,686,868-88,687,061 BMPR1A
    nsv5910497copy number variation1nstd209human GRCh38 chr10: 86,805,900-86,805,978 , GRCh37.p13 chr10: 88,565,657-88,565,735 BMPR1A
    nsv5700775mobile element insertion1nstd211human GRCh38 chr10: 86,864,757-86,864,757 , GRCh37.p13 chr10: 88,624,514-88,624,514 BMPR1A
    nsv5699664mobile element insertion2nstd211human GRCh38 chr10: 86,906,762-86,906,762 , GRCh37.p13 chr10: 88,666,519-88,666,519 BMPR1A
    nsv5699138mobile element insertion1nstd211human GRCh38 chr10: 86,790,189-86,790,189 , GRCh37.p13 chr10: 88,549,946-88,549,946 BMPR1A
    nsv5672765copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,651,874-88,651,996 , GRCh38.p12 chr10: 86,892,117-86,892,239 BMPR1A
    nsv5672693copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,598,623-88,659,889 , GRCh38.p12 chr10: 86,838,866-86,900,132 BMPR1A, RPAP2P1, 1 more genes
    nsv5672692copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,598,623-88,635,852 , GRCh38.p12 chr10: 86,838,866-86,876,095 RPAP2P1, BMPR1A
    nsv5672610copy number variation1nstd102humanPathogenic GRCh37 chr10: 88,683,123-89,725,321 , GRCh38.p12 chr10: 86,923,366-87,965,564 FAM245A, BMPR1A, 30 more genes
    nsv5672533copy number variation1nstd102humanLikely pathogenic GRCh37 chr10: 88,671,987-88,683,476 , GRCh38.p12 chr10: 86,912,230-86,923,719 BMPR1A
    nsv5644438insertion1nstd207human GRCh38 chr10: 86,865,229-86,865,229 , GRCh37.p13 chr10: 88,624,986-88,624,986 BMPR1A
    nsv5633834insertion1nstd207human GRCh38 chr10: 86,791,687-86,791,687 , GRCh37.p13 chr10: 88,551,444-88,551,444 BMPR1A
    nsv5600991copy number variation1nstd207human GRCh38 chr10: 86,906,418-86,906,757 , GRCh37.p13 chr10: 88,666,175-88,666,514 BMPR1A
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