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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099176copy number variation1nstd231human GRCh38.p12 chr1: 10,224,807-12,488,948 , GRCh37 chr1: 10,284,865-12,549,002 TNFRSF8, CLCN6, 64 more genes
    nsv7098827copy number variation1nstd102humanPathogenic GRCh37 chr1: 4,481,271-20,530,242 , GRCh38.p12 chr1: 4,421,211-20,203,749 LOC107985467, LINC01777, 386 more genes
    nsv7096008copy number variation1nstd102humanUncertain significance GRCh37 chr1: 9,304,994-12,569,078 , GRCh38.p12 chr1: 9,244,935-12,509,024 NMNAT1, DISP3, 91 more genes
    nsv7057525inversion1nstd229human GRCh38 chr1: 7,829,944-15,116,659 , GRCh37.p13 chr1: 7,890,004-15,443,155 PEX14, RNU6-304P, 187 more genes
    nsv7052549inversion1nstd229human GRCh38 chr1: 8,322,830-13,737,741 , GRCh37.p13 chr1: 8,382,890-14,064,236 MIR4632, PLOD1, 166 more genes
    nsv7048193inversion1nstd229human GRCh38 chr1: 9,469,567-16,279,388 , GRCh37.p13 chr1: 9,529,626-16,605,883 PRAMEF36P, HNRNPCL3, 193 more genes
    nsv7047983inversion1nstd229human GRCh38 chr1: 5,346,988-12,521,611 , GRCh37.p13 chr1: 5,407,048-12,581,655 THAP3, UBIAD1, 165 more genes
    nsv7046461inversion1nstd229human GRCh38 chr1: 5,352,168-12,521,473 , GRCh37.p13 chr1: 5,412,228-12,581,517 LINC02606, C1orf127, 165 more genes
    nsv6657761copy number variation1nstd229human GRCh38 chr1: 9,535,063-15,753,073 , GRCh37.p13 chr1: 9,595,122-16,079,568 SLC25A34-AS1, TMEM274P, 173 more genes
    nsv6641236copy number variation1nstd229human GRCh38 chr1: 12,202,171-12,206,736 , GRCh37.p13 chr1: 12,262,228-12,266,793 TNFRSF1B
    nsv6641235copy number variation1nstd229human GRCh38 chr1: 12,193,100-12,201,966 , GRCh37.p13 chr1: 12,253,157-12,262,023 TNFRSF1B
    nsv6641234copy number variation1nstd229human GRCh38 chr1: 12,192,097-12,205,343 , GRCh37.p13 chr1: 12,252,154-12,265,400 TNFRSF1B, MIR4632
    nsv6641233copy number variation1nstd229human GRCh38 chr1: 12,185,095-12,185,126 , GRCh37.p13 chr1: 12,245,152-12,245,183 TNFRSF1B
    nsv6641232copy number variation1nstd229human GRCh38 chr1: 12,175,159-12,178,920 , GRCh37.p13 chr1: 12,235,216-12,238,977 TNFRSF1B
    nsv6640982copy number variation1nstd229human GRCh38 chr1: 11,872,601-12,215,400 , GRCh37.p13 chr1: 11,932,658-12,275,457 TNFRSF8, RNU6-777P, 13 more genes
    nsv6640305copy number variation1nstd229human GRCh38 chr1: 11,514,401-12,295,600 , GRCh37.p13 chr1: 11,574,458-12,355,657 PLOD1, MIR4632, 31 more genes
    nsv6638770copy number variation1nstd229human GRCh38 chr1: 10,461,501-12,236,800 , GRCh37.p13 chr1: 10,521,558-12,296,857 RN7SL614P, CFL1P6, 57 more genes
    nsv6637093copy number variation1nstd102humanPathogenic GRCh37 chr1: 849,467-12,448,956 , GRCh38.p12 chr1: 914,087-12,388,897 VWA1, CEP104, 311 more genes
    nsv6636785copy number variation1nstd102humanPathogenic GRCh37 chr1: 6,758,933-19,287,770 , GRCh38.p12 chr1: 6,698,873-18,961,276 GPR157, MST1L, 313 more genes
    nsv6317793copy number variation1nstd223human GRCh38 chr1: 12,185,095-12,185,125 , GRCh37.p13 chr1: 12,245,152-12,245,182 TNFRSF1B
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