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Items: 1 to 20 of 184

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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
    nsv7095316copy number variation1nstd102humanUncertain significance GRCh37 chr1: 11,269,349-11,346,188 , GRCh38.p12 chr1: 11,209,292-11,286,131 MTOR, UBE2V2P3, 3 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
    nsv6640311copy number variation1nstd229human GRCh38 chr1: 11,263,728-11,276,819 , GRCh37.p13 chr1: 11,323,785-11,336,876 UBE2V2P3, UBIAD1, 1 more genes
    nsv6640235copy number variation1nstd229human GRCh38 chr1: 11,292,628-11,306,168 , GRCh37.p13 chr1: 11,352,685-11,366,225 UBIAD1
    nsv6640129copy number variation1nstd229human GRCh38 chr1: 11,296,614-11,300,026 , GRCh37.p13 chr1: 11,356,671-11,360,083 UBIAD1
    nsv6640127copy number variation1nstd229human GRCh38 chr1: 11,295,590-11,304,096 , GRCh37.p13 chr1: 11,355,647-11,364,153 UBIAD1
    nsv6640123copy number variation1nstd229human GRCh38 chr1: 11,281,526-11,295,219 , GRCh37.p13 chr1: 11,341,583-11,355,276 UBIAD1
    nsv6639968copy number variation1nstd229human GRCh38 chr1: 11,208,326-11,435,015 , GRCh37.p13 chr1: 11,268,383-11,495,072 UBIAD1, LOC105376737, 7 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
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