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Items: 1 to 20 of 146

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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
    nsv7095738copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,753,911-11,854,615 , GRCh38.p12 chr1: 10,693,854-11,794,558 MAD2L2, HSPE1P24, 33 more genes
    nsv7095692copy number variation1nstd102humanUncertain significance GRCh37 chr1: 10,698,999-11,907,741 , GRCh38.p12 chr1: 10,638,942-11,847,684 MTHFR, UBIAD1, 36 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
    nsv6640643copy number variation1nstd229human GRCh38 chr1: 11,603,401-11,616,200 , GRCh37.p13 chr1: 11,663,458-11,676,257 LINC01647
    nsv6640633copy number variation1nstd229human GRCh38 chr1: 11,579,201-11,613,000 , GRCh37.p13 chr1: 11,639,258-11,673,057 LINC01647
    nsv6640463copy number variation1nstd229human GRCh38 chr1: 11,604,645-11,630,565 , GRCh37.p13 chr1: 11,664,702-11,690,622 LINC01647
    nsv6640428copy number variation1nstd229human GRCh38 chr1: 11,535,192-11,661,508 , GRCh37.p13 chr1: 11,595,249-11,721,565 FBXO2, LINC01647, 2 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
    nsv6640255copy number variation1nstd229human GRCh38 chr1: 11,350,419-11,656,941 , GRCh37.p13 chr1: 11,410,476-11,716,998 LOC105376739, MTCYBP45, 5 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
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