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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5956594insertion1nstd209human GRCh38 chr5: 98,988,759-98,988,759 , GRCh37.p13 chr5: 98,324,463-98,324,463 CHD1-DT
    nsv5895294copy number variation1nstd209human GRCh38 chr5: 98,958,311-98,958,614 , GRCh37.p13 chr5: 98,294,015-98,294,318 CHD1-DT
    nsv5843922copy number variation1nstd209human GRCh38 chr5: 98,946,497-98,947,701 , GRCh37.p13 chr5: 98,282,201-98,283,405 CHD1-DT
    nsv5678974mobile element insertion2nstd211human GRCh38 chr5: 98,962,011-98,962,011 , GRCh37.p13 chr5: 98,297,715-98,297,715 CHD1-DT
    nsv5676175mobile element insertion1nstd211human GRCh38 chr5: 98,936,639-98,936,639 , GRCh37.p13 chr5: 98,272,343-98,272,343 CHD1-DT
    nsv5641455insertion1nstd207human GRCh38 chr5: 98,988,746-98,988,746 , GRCh37.p13 chr5: 98,324,450-98,324,450 CHD1-DT
    nsv5635928insertion1nstd207human GRCh38 chr5: 98,988,714-98,988,714 , GRCh37.p13 chr5: 98,324,418-98,324,418 CHD1-DT
    nsv5634422insertion1nstd207human GRCh38 chr5: 98,988,699-98,988,699 , GRCh37.p13 chr5: 98,324,403-98,324,403 CHD1-DT
    nsv5459534copy number variation1nstd206human GRCh38 chr5: 98,978,462-98,979,035 , GRCh37.p13 chr5: 98,314,166-98,314,739 CHD1-DT
    nsv5399833mobile element insertion1nstd206human GRCh38 chr5: 98,962,011-98,962,062 , GRCh37.p13 chr5: 98,297,715-98,297,766 CHD1-DT
    nsv5098634mobile element insertion1nstd203human GRCh38 chr5: 98,978,983-98,978,983 , GRCh37.p13 chr5: 98,314,687-98,314,687 CHD1-DT
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4931714copy number variation1nstd200human GRCh38 chr5: 98,970,723-98,971,548 , GRCh37.p13 chr5: 98,306,427-98,307,252 CHD1-DT
    nsv4931713copy number variation1nstd200human GRCh38 chr5: 98,938,017-98,938,599 , GRCh37.p13 chr5: 98,273,721-98,274,303 CHD1-DT
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 more genes
    nsv4793435copy number variation1nstd200human GRCh37 chr5: 98,306,427-98,307,252 , GRCh38.p12 chr5: 98,970,723-98,971,548 CHD1-DT
    nsv4793434copy number variation1nstd200human GRCh37 chr5: 98,294,014-98,294,329 , GRCh38.p12 chr5: 98,958,310-98,958,625 CHD1-DT
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