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Items: 1 to 20 of 371

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6137666copy number variation1nstd102humanPathogenic GRCh37 chrX: 91,829,757-113,050,225 , GRCh38.p12 chrX: 92,574,758-113,806,943 TCEAL8, MTND5P26, 272 more genes
    nsv6129946mobile element insertion1nstd186human GRCh37 chrX: 106,835,954-106,835,962 , GRCh38.p12 chrX: 107,592,724-107,592,732 FRMPD3
    nsv6113767mobile element insertion1nstd186human GRCh37 chrX: 106,813,473-106,813,473 , GRCh38.p12 chrX: 107,570,243-107,570,243 FRMPD3
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5959325insertion1nstd209human GRCh38 chrX: 107,592,724-107,592,724 , GRCh37.p13 chrX: 106,835,954-106,835,954 FRMPD3
    nsv5949335insertion1nstd209human GRCh38 chrX: 107,570,243-107,570,243 , GRCh37.p13 chrX: 106,813,473-106,813,473 FRMPD3
    nsv5875082copy number variation1nstd209human GRCh38 chrX: 107,601,468-107,601,521 , GRCh37.p13 chrX: 106,844,698-106,844,751 FRMPD3
    nsv5724095mobile element insertion2nstd211human GRCh38 chrX: 107,592,724-107,592,724 , GRCh37.p13 chrX: 106,835,954-106,835,954 FRMPD3
    nsv5722295mobile element insertion2nstd211human GRCh38 chrX: 107,570,257-107,570,257 , GRCh37.p13 chrX: 106,813,487-106,813,487 FRMPD3
    nsv5718823mobile element insertion2nstd211human GRCh38 chrX: 107,538,830-107,538,830 , GRCh37.p13 chrX: 106,782,060-106,782,060 FRMPD3-AS1, FRMPD3
    nsv5616216insertion1nstd207human GRCh38 chrX: 107,592,724-107,592,724 , GRCh37.p13 chrX: 106,835,954-106,835,954 FRMPD3
    nsv5612959insertion1nstd207human GRCh38 chrX: 107,583,788-107,583,788 , GRCh37.p13 chrX: 106,827,018-106,827,018 FRMPD3
    nsv5606398insertion1nstd207human GRCh38 chrX: 107,570,243-107,570,243 , GRCh37.p13 chrX: 106,813,473-106,813,473 FRMPD3
    nsv5563500mobile element insertion1nstd206human GRCh38 chrX: 107,570,243-107,570,243 , GRCh37.p13 chrX: 106,813,473-106,813,473 FRMPD3
    nsv5557463mobile element insertion1nstd206human GRCh38 chrX: 107,592,724-107,592,732 , GRCh37.p13 chrX: 106,835,954-106,835,962 FRMPD3
    nsv5433242copy number variation1nstd206human GRCh38 chrX: 107,537,558-107,537,621 , GRCh37.p13 chrX: 106,780,788-106,780,851 FRMPD3, FRMPD3-AS1
    nsv5415558copy number variation1nstd206human GRCh38 chrX: 107,604,505-107,604,781 , GRCh37.p13 chrX: 106,847,735-106,848,011 FRMPD3
    nsv5376851translocation1nstd200human GRCh38 chrX: 107,534,917-107,534,917 , GRCh38 chrX: 107,535,032-107,535,032 , GRCh37.p13 chrX: 106,778,262-106,778,262 , GRCh37.p13 chrX: 106,778,147-106,778,147 FRMPD3, FRMPD3-AS1
    nsv5341184translocation1nstd200human GRCh37 chr6: 120,507,468-120,507,468 , GRCh37 chrX: 106,846,497-106,846,497 , GRCh38.p12 chrX: 107,603,267-107,603,267 , GRCh38.p12 chr6: 120,186,322-120,186,322 FRMPD3
    nsv5329655translocation1nstd200human GRCh37 chrX: 106,778,262-106,778,262 , GRCh37 chrX: 106,778,148-106,778,148 , GRCh38.p12 chrX: 107,535,032-107,535,032 , GRCh38.p12 chrX: 107,534,918-107,534,918 FRMPD3, FRMPD3-AS1
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