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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976992insertion1nstd209human GRCh38 chr11: 63,410,257-63,410,257 , GRCh37.p13 chr11: 63,177,729-63,177,729 SLC22A9
    nsv5970855insertion1nstd209human GRCh38 chr11: 63,378,230-63,378,230 , GRCh37.p13 chr11: 63,145,702-63,145,702 SLC22A9
    nsv5923154copy number variation1nstd209human GRCh38 chr11: 63,374,968-63,375,028 , GRCh37.p13 chr11: 63,142,440-63,142,500 SLC22A9
    nsv5851203copy number variation1nstd209human GRCh38 chr11: 63,387,118-63,388,617 , GRCh37.p13 chr11: 63,154,590-63,156,089 SLC22A9
    nsv5701290mobile element insertion2nstd211human GRCh38 chr11: 63,378,242-63,378,242 , GRCh37.p13 chr11: 63,145,714-63,145,714 SLC22A9
    nsv5696304mobile element insertion2nstd211human GRCh38 chr11: 63,392,388-63,392,388 , GRCh37.p13 chr11: 63,159,860-63,159,860 SLC22A9
    nsv5649260insertion1nstd207human GRCh38 chr11: 63,378,230-63,378,230 , GRCh37.p13 chr11: 63,145,702-63,145,702 SLC22A9
    nsv5547277insertion1nstd206human GRCh38 chr11: 63,378,242-63,378,281 , GRCh37.p13 chr11: 63,145,714-63,145,753 SLC22A9
    nsv5496666copy number variation1nstd206human GRCh38 chr11: 63,379,014-63,379,575 , GRCh37.p13 chr11: 63,146,486-63,147,047 SLC22A9
    nsv5395780mobile element insertion1nstd206human GRCh38 chr11: 63,392,388-63,392,439 , GRCh37.p13 chr11: 63,159,860-63,159,911 SLC22A9
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5355273translocation1nstd200human GRCh38 chr11: 63,379,575-63,379,575 , GRCh38 chr11: 63,379,014-63,379,014 , GRCh37.p13 chr11: 63,146,486-63,146,486 , GRCh37.p13 chr11: 63,147,047-63,147,047 SLC22A9
    nsv5355272translocation1nstd200human GRCh38 chr11: 63,375,037-63,375,037 , GRCh38 chr11: 63,374,968-63,374,968 , GRCh37.p13 chr11: 63,142,440-63,142,440 , GRCh37.p13 chr11: 63,142,509-63,142,509 SLC22A9
    nsv5333484translocation1nstd200human GRCh37 chr11: 63,142,440-63,142,440 , GRCh37 chr11: 63,142,509-63,142,509 , GRCh38.p12 chr11: 63,374,968-63,374,968 , GRCh38.p12 chr11: 63,375,037-63,375,037 SLC22A9
    nsv5194806mobile element insertion1nstd203human GRCh38 chr11: 63,369,784-63,369,787 , GRCh37.p13 chr11: 63,137,256-63,137,259 SLC22A9
    nsv5190559mobile element insertion1nstd203human GRCh38 chr11: 63,403,470-63,403,486 , GRCh37.p13 chr11: 63,170,942-63,170,958 SLC22A9
    nsv5139807mobile element insertion1nstd203human GRCh38 chr11: 63,378,235-63,378,242 , GRCh37.p13 chr11: 63,145,707-63,145,714 SLC22A9
    nsv5134069mobile element insertion1nstd203human GRCh38 chr11: 63,378,232-63,378,242 , GRCh37.p13 chr11: 63,145,704-63,145,714 SLC22A9
    nsv5127370mobile element insertion1nstd203human GRCh38 chr11: 63,378,229-63,378,242 , GRCh37.p13 chr11: 63,145,701-63,145,714 SLC22A9
    nsv5126521mobile element insertion1nstd203human GRCh38 chr11: 63,378,234-63,378,242 , GRCh37.p13 chr11: 63,145,706-63,145,714 SLC22A9
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