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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
    nsv7095702copy number variation1nstd102humanPathogenic GRCh37 chr1: 12,049,226-12,065,004 , GRCh38.p12 chr1: 11,989,169-12,004,947 MFN2
    nsv7095700copy number variation1nstd102humanUncertain significance GRCh37 chr1: 11,906,066-12,066,770 , GRCh38.p12 chr1: 11,846,009-12,006,713 NPPB, PLOD1, 7 more genes
    nsv7095699copy number variation1nstd102humanUncertain significance GRCh37 chr1: 11,847,760-12,066,770 , GRCh38.p12 chr1: 11,787,703-12,006,713 MTHFR, NPPB, 10 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
    nsv6641214copy number variation1nstd229human GRCh38 chr1: 11,990,083-11,992,358 , GRCh37.p13 chr1: 12,050,140-12,052,415 MFN2
    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
    nsv6640782copy number variation1nstd229human GRCh38 chr1: 11,949,697-12,005,360 , GRCh37.p13 chr1: 12,009,754-12,065,417 PLOD1, MFN2
    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
    nsv6328504copy number variation1nstd223human GRCh38 chr1: 11,998,170-11,999,609 , GRCh37.p13 chr1: 12,058,227-12,059,666 MFN2
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