U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Links from Gene

Items: 1 to 20 of 180

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7073074inversion1nstd229human GRCh38 chr14: 99,646,022-99,727,066 , GRCh37.p13 chr14: 100,112,359-100,193,403 CYP46A1, HHIPL1
    nsv7071767inversion1nstd229human GRCh38 chr14: 99,706,574-99,848,441 , GRCh37.p13 chr14: 100,172,911-100,314,778 EML1, CYP46A1
    nsv7068889inversion1nstd229human GRCh38 chr14: 99,706,773-99,708,894 , GRCh37.p13 chr14: 100,173,110-100,175,231 CYP46A1
    nsv6972475copy number variation1nstd229human GRCh38 chr14: 99,175,901-99,949,300 , GRCh37.p13 chr14: 99,642,238-100,415,637 SETD3, LOC105370661, 10 more genes
    nsv6972243copy number variation1nstd229human GRCh38 chr14: 98,444,126-100,047,287 , GRCh37.p13 chr14: 98,910,463-100,513,624 CYP46A1, RPS2P3, 19 more genes
    nsv6968255copy number variation1nstd229human GRCh38 chr14: 99,175,601-99,684,700 , GRCh37.p13 chr14: 99,641,938-100,151,037 BCL11B, CCDC85C, 7 more genes
    nsv6960784copy number variation1nstd229human GRCh38 chr14: 99,675,201-99,684,800 , GRCh37.p13 chr14: 100,141,538-100,151,137 HHIPL1, CYP46A1
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
    nsv6590551inversion1nstd223human GRCh38 chr14: 99,646,022-99,727,066 , GRCh37.p13 chr14: 100,112,359-100,193,403 CYP46A1, HHIPL1
    nsv6586868inversion1nstd223human GRCh38 chr14: 99,721,732-99,726,473 , GRCh37.p13 chr14: 100,188,069-100,192,810 CYP46A1
    nsv6506619copy number variation1nstd223human GRCh38 chr14: 99,634,053-99,695,864 , GRCh37.p13 chr14: 100,100,390-100,162,201 HHIPL1, CYP46A1
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6291768copy number variation1nstd102humanPathogenic GRCh37 chr14: 95,871,795-102,457,523 , GRCh38.p12 chr14: 95,405,458-101,991,186 CCDC85C, MEG3, 206 more genes
    nsv6198490copy number variation1nstd214human GRCh38 chr14: 99,708,208-99,708,316 , GRCh37.p13 chr14: 100,174,545-100,174,653 CYP46A1
    nsv6190665copy number variation1nstd214human GRCh38 chr14: 99,708,335-99,708,556 , GRCh37.p13 chr14: 100,174,672-100,174,893 CYP46A1
    nsv6189501copy number variation1nstd214human GRCh38 chr14: 99,708,475-99,708,585 , GRCh37.p13 chr14: 100,174,812-100,174,922 CYP46A1
    nsv6132885copy number variation1nstd213human GRCh37 chr14: 99,590,000-101,630,001 , GRCh38.p12 chr14: 99,123,663-101,163,664 DLK1, MEG8, 135 more genes
    nsv6096349insertion1nstd212human GRCh38 chr14: 99,695,943-99,695,943 , GRCh37.p13 chr14: 100,162,280-100,162,280 CYP46A1
    nsv6034834copy number variation1nstd212human GRCh38 chr14: 99,708,212-99,708,320 , GRCh37.p13 chr14: 100,174,549-100,174,657 CYP46A1
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Find related data

    Recent activity

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    Support Center