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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
    nsv7098897copy number variation1nstd102humanPathogenic GRCh37 chr15: 67,358,491-91,644,328 , GRCh38.p12 chr15: 67,066,153-91,101,098 LINC00933, DNM1P9, 540 more genes
    nsv7070270inversion1nstd229human GRCh38 chr15: 70,870,846-78,233,029 , GRCh37.p13 chr15: 71,163,185-78,525,371 GOLGA6C, LOC102723657, 178 more genes
    nsv7069747inversion1nstd229human GRCh38 chr15: 65,994,863-75,247,978 , GRCh37.p13 chr15: 66,287,201-75,540,319 REC114, PARP6, 199 more genes
    nsv7059031inversion1nstd229human GRCh38 chr15: 70,160,153-73,809,878 , GRCh37.p13 chr15: 70,452,492-74,102,219 CD276, LOC107984716, 71 more genes
    nsv6975774copy number variation1nstd229human GRCh38 chr15: 71,685,763-71,689,710 , GRCh37.p13 chr15: 71,978,102-71,982,049 THSD4, THSD4-AS2
    nsv6974038copy number variation1nstd229human GRCh38 chr15: 71,687,401-71,696,500 , GRCh37.p13 chr15: 71,979,740-71,988,839 THSD4-AS2, THSD4
    nsv6967679copy number variation1nstd229human GRCh38 chr15: 71,405,372-71,707,393 , GRCh37.p13 chr15: 71,697,711-71,999,732 LOC107984716, THSD4-AS2, 1 more genes
    nsv6964281copy number variation1nstd229human GRCh38 chr15: 71,684,201-71,690,200 , GRCh37.p13 chr15: 71,976,540-71,982,539 THSD4-AS2, THSD4
    nsv6960334copy number variation1nstd229human GRCh38 chr15: 71,688,313-71,693,367 , GRCh37.p13 chr15: 71,980,652-71,985,706 THSD4-AS2, THSD4
    nsv6637379copy number variation1nstd102humanUncertain significance GRCh37 chr15: 71,747,077-71,980,686 , GRCh38.p12 chr15: 71,454,738-71,688,347 LOC107984716, THSD4-AS2, 1 more genes
    nsv6146143copy number variation1nstd206human GRCh38 chr15: 71,688,336-71,699,292 , GRCh37.p13 chr15: 71,980,675-71,991,631 THSD4-AS2, THSD4
    nsv6132961copy number variation1nstd213human GRCh37 chr15: 69,080,000-73,430,001 , GRCh38.p12 chr15: 68,787,661-73,137,660 BBS4, MYO9A, 84 more genes
    nsv5933606copy number variation1nstd209human GRCh38 chr15: 71,577,714-80,433,232 , GRCh37.p13 chr15: 71,870,053-80,725,573 , STRA6, 229 more genes
    nsv5707440mobile element insertion1nstd211human GRCh38 chr15: 71,688,292-71,688,292 , GRCh37.p13 chr15: 71,980,631-71,980,631 THSD4, THSD4-AS2
    nsv5603779copy number variation1nstd207human GRCh38 chr15: 71,688,304-71,699,209 , GRCh37.p13 chr15: 71,980,643-71,991,548 THSD4-AS2, THSD4
    nsv5426413mobile element insertion1nstd206human GRCh38 chr15: 71,688,292-71,688,343 , GRCh37.p13 chr15: 71,980,631-71,980,682 THSD4-AS2, THSD4
    nsv5380758copy number variation2nstd102humanUncertain significance GRCh37 chr15: 32,964,879-91,358,519 , GRCh38.p12 chr15: 32,672,678-90,815,289 LOC105370794, HNRNPA1P45, 1173 more genes
    nsv4728893copy number variation1nstd102humanLikely pathogenic GRCh37 chr15: 70,268,937-74,098,081 , GRCh38.p12 chr15: 69,976,598-73,805,740 BBS4, FKBP1AP2, 75 more genes
    nsv4634108copy number variation1nstd183human GRCh37 chr15: 71,945,010-72,272,867 , GRCh38.p12 chr15: 71,652,671-71,980,526 MYO9A, NR2E3, 4 more genes
    nsv4338323sequence alteration1nstd166human GRCh37.p13 chr15: 69,446,476-72,211,091 , GRCh38.p12 chr15: 69,154,137-71,918,750 , MYO9A, 45 more genes
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