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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148081copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,167,260-12,533,766 , GRCh38.p12 chr3: 10,125,576-12,492,267 SLC6A1-AS1, LOC101927467, 37 more genes
    nsv7056701inversion1nstd229human GRCh38 chr3: 11,170,781-11,377,104 , GRCh37.p13 chr3: 11,212,467-11,418,578 CHCHD4P4, HRH1, 2 more genes
    nsv7055847inversion1nstd229human GRCh38 chr3: 5,111,802-11,290,661 , GRCh37.p13 chr3: 5,153,487-11,332,347 GHRLOS, LHFPL4, 96 more genes
    nsv7051015inversion1nstd229human GRCh38 chr3: 11,361,240-11,365,287 , GRCh37.p13 chr3: 11,402,714-11,406,761 ATG7
    nsv7049223inversion1nstd229human GRCh38 chr3: 11,398,199-11,398,221 , GRCh37.p13 chr3: 11,439,673-11,439,695 ATG7
    nsv7043780inversion1nstd229human GRCh38 chr3: 11,503,945-11,515,779 , GRCh37.p13 chr3: 11,545,419-11,557,253 ATG7
    nsv7042755inversion1nstd229human GRCh38 chr3: 8,982,205-12,221,239 , GRCh37.p13 chr3: 9,023,889-12,262,739 SYN2, MTCO1P5, 74 more genes
    nsv6716891copy number variation1nstd229human GRCh38 chr3: 11,368,701-11,373,300 , GRCh37.p13 chr3: 11,410,175-11,414,774 ATG7
    nsv6715841copy number variation1nstd229human GRCh38 chr3: 11,457,102-11,474,243 , GRCh37.p13 chr3: 11,498,576-11,515,717 ATG7
    nsv6715774copy number variation1nstd229human GRCh38 chr3: 11,402,511-11,485,561 , GRCh37.p13 chr3: 11,443,985-11,527,035 ATG7
    nsv6714569copy number variation1nstd229human GRCh38 chr3: 11,498,101-11,503,592 , GRCh37.p13 chr3: 11,539,575-11,545,066 ATG7
    nsv6714556copy number variation1nstd229human GRCh38 chr3: 11,290,797-11,290,930 , GRCh37.p13 chr3: 11,332,483-11,332,616 ATG7
    nsv6713930copy number variation1nstd229human GRCh38 chr3: 11,176,966-11,396,655 , GRCh37.p13 chr3: 11,218,652-11,438,129 CHCHD4P4, ATG7, 2 more genes
    nsv6713919copy number variation1nstd229human GRCh38 chr3: 11,501,973-11,519,809 , GRCh37.p13 chr3: 11,543,447-11,561,283 ATG7
    nsv6713641copy number variation1nstd229human GRCh38 chr3: 11,511,856-11,513,575 , GRCh37.p13 chr3: 11,553,330-11,555,049 ATG7
    nsv6713322copy number variation1nstd229human GRCh38 chr3: 11,525,105-11,525,585 , GRCh37.p13 chr3: 11,566,579-11,567,059 ATG7
    nsv6713089copy number variation1nstd229human GRCh38 chr3: 11,463,812-11,464,393 , GRCh37.p13 chr3: 11,505,286-11,505,867 ATG7
    nsv6712424copy number variation1nstd229human GRCh38 chr3: 11,451,149-11,453,174 , GRCh37.p13 chr3: 11,492,623-11,494,648 ATG7
    nsv6712284copy number variation1nstd229human GRCh38 chr3: 11,412,154-11,421,665 , GRCh37.p13 chr3: 11,453,628-11,463,139 ATG7
    nsv6712118copy number variation1nstd229human GRCh38 chr3: 11,563,146-11,563,176 , GRCh37.p13 chr3: 11,604,620-11,604,650 ATG7, VGLL4
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