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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7078062inversion1nstd229human GRCh38 chr9: 99,955,191-100,728,757 , GRCh37.p13 chr9: 102,717,473-103,491,039 CAVIN4, UPF3AP3, 13 more genes
    nsv7075759inversion1nstd229human GRCh38 chr9: 99,912,130-99,915,490 , GRCh37.p13 chr9: 102,674,412-102,677,772 STX17
    nsv7075365inversion1nstd229human GRCh38 chr9: 94,549,389-100,549,990 , GRCh37.p13 chr9: 97,311,671-103,312,272 PCAT7, ANKS6, 128 more genes
    nsv6876578copy number variation1nstd229human GRCh38 chr9: 99,969,101-99,971,500 , GRCh37.p13 chr9: 102,731,383-102,733,782 STX17
    nsv6874790copy number variation1nstd229human GRCh38 chr9: 99,928,843-99,951,057 , GRCh37.p13 chr9: 102,691,125-102,713,339 STX17
    nsv6873702copy number variation1nstd229human GRCh38 chr9: 99,910,205-99,918,721 , GRCh37.p13 chr9: 102,672,487-102,681,003 STX17
    nsv6869643copy number variation1nstd229human GRCh38 chr9: 99,971,883-99,973,343 , GRCh37.p13 chr9: 102,734,165-102,735,625 STX17
    nsv6868656copy number variation1nstd229human GRCh38 chr9: 99,937,036-99,937,298 , GRCh37.p13 chr9: 102,699,318-102,699,580 STX17
    nsv6867225copy number variation1nstd229human GRCh38 chr9: 99,933,686-99,937,865 , GRCh37.p13 chr9: 102,695,968-102,700,147 STX17
    nsv6865193copy number variation1nstd229human GRCh38 chr9: 99,949,370-99,949,983 , GRCh37.p13 chr9: 102,711,652-102,712,265 STX17
    nsv6862570copy number variation1nstd229human GRCh38 chr9: 99,929,262-99,933,542 , GRCh37.p13 chr9: 102,691,544-102,695,824 STX17
    nsv6860633copy number variation1nstd229human GRCh38 chr9: 99,922,677-99,927,815 , GRCh37.p13 chr9: 102,684,959-102,690,097 STX17
    nsv6860593copy number variation1nstd229human GRCh38 chr9: 99,919,901-99,927,300 , GRCh37.p13 chr9: 102,682,183-102,689,582 STX17
    nsv6859596copy number variation1nstd229human GRCh38 chr9: 99,966,409-99,972,036 , GRCh37.p13 chr9: 102,728,691-102,734,318 STX17
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6558336inversion1nstd223human GRCh38 chr9: 99,955,191-100,728,759 , GRCh37.p13 chr9: 102,717,473-103,491,041 RPS2P35, STX17, 13 more genes
    nsv6454283copy number variation1nstd223human GRCh38 chr9: 99,950,646-99,951,162 , GRCh37.p13 chr9: 102,712,928-102,713,444 STX17
    nsv6453459copy number variation1nstd223human GRCh38 chr9: 99,932,301-99,933,200 , GRCh37.p13 chr9: 102,694,583-102,695,482 STX17
    nsv6453168copy number variation1nstd223human GRCh38 chr9: 99,954,579-99,955,014 , GRCh37.p13 chr9: 102,716,861-102,717,296 STX17
    nsv6452022copy number variation1nstd223human GRCh38 chr9: 99,962,956-99,963,908 , GRCh37.p13 chr9: 102,725,238-102,726,190 STX17
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