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Items: 1 to 20 of 233

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099247copy number variation1nstd231human GRCh38.p12 chr1: 171,697,692-172,567,791 , GRCh37 chr1: 171,666,832-172,536,931 PIGC, VAMP4, 16 more genes
    nsv7095763copy number variation1nstd102humanUncertain significance GRCh37 chr1: 172,410,869-172,411,762 , GRCh38.p12 chr1: 172,441,729-172,442,622 LOC102724528, C1orf105, 1 more genes
    nsv7043069inversion1nstd229human GRCh38 chr1: 172,366,106-172,496,936 , GRCh37.p13 chr1: 172,335,246-172,466,076 C1orf105, PIGC, 3 more genes
    nsv7042181inversion1nstd229human GRCh38 chr1: 172,428,212-172,433,928 , GRCh37.p13 chr1: 172,397,352-172,403,068 LOC102724528, C1orf105
    nsv6644791copy number variation1nstd229human GRCh38 chr1: 172,447,501-172,448,500 , GRCh37.p13 chr1: 172,416,641-172,417,640 C1orf105, LOC102724528
    nsv6644765copy number variation1nstd229human GRCh38 chr1: 171,564,330-172,954,419 , GRCh37.p13 chr1: 171,533,469-172,923,559 LOC107985225, RPS15P3, 27 more genes
    nsv6644714copy number variation1nstd229human GRCh38 chr1: 172,420,186-172,427,119 , GRCh37.p13 chr1: 172,389,326-172,396,259 LOC102724528, C1orf105
    nsv6644345copy number variation1nstd229human GRCh38 chr1: 172,424,069-172,425,305 , GRCh37.p13 chr1: 172,393,209-172,394,445 LOC102724528, C1orf105
    nsv6636969copy number variation1nstd102humanUncertain significance GRCh37 chr1: 172,268,908-172,389,345 , GRCh38.p12 chr1: 172,299,768-172,420,205 RNU6-157P, LOC102724528, 2 more genes
    nsv6636413copy number variation1nstd102humanUncertain significance GRCh37 chr1: 172,365,330-172,399,870 , GRCh38.p12 chr1: 172,396,190-172,430,730 C1orf105, DNM3, 1 more genes
    nsv6636272copy number variation1nstd102humanUncertain significance GRCh37 chr1: 172,399,416-172,468,762 , GRCh38.p12 chr1: 172,430,276-172,499,622 PIGC, LOC102724528, 1 more genes
    nsv6634366copy number variation1nstd102humanUncertain significance GRCh37 chr1: 171,649,657-172,399,870 , GRCh38.p12 chr1: 171,680,517-172,430,730 RNU6-157P, C1orf105, 15 more genes
    nsv6329275copy number variation1nstd223human GRCh38 chr1: 172,444,726-172,445,879 , GRCh37.p13 chr1: 172,413,866-172,415,019 C1orf105, LOC102724528
    nsv6313519copy number variation1nstd102humanPathogenic GRCh37 chr1: 171,881,608-175,899,893 , GRCh38.p12 chr1: 171,912,468-175,930,757 RNU6-693P, PIGC, 73 more genes
    nsv6310765copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr1: 171,605,065-173,962,123 , GRCh38.p12 chr1: 171,635,925-173,992,985 RNU6-157P, SNORD47, 60 more genes
    nsv6300606copy number variation1nstd186human GRCh37 chr1: 172,437,881-172,438,220 , GRCh38.p12 chr1: 172,468,741-172,469,080 C1orf105
    nsv6133947copy number variation1nstd213human GRCh37 chr1: 172,350,000-172,520,001 , GRCh38.p12 chr1: 172,380,860-172,550,861 PIGC, DNM3, 3 more genes
    nsv6133940copy number variation1nstd213human GRCh37 chr1: 170,740,000-173,330,001 , GRCh38.p12 chr1: 170,770,859-173,360,862 TNFSF4, VAMP4, 50 more genes
    nsv6133933copy number variation1nstd213human GRCh37 chr1: 161,620,000-196,730,001 , GRCh38.p12 chr1: 161,650,210-196,760,871 FASLG, SERPINC1, 510 more genes
    nsv6133567copy number variation1nstd213human GRCh37 chr1: 170,760,000-174,730,001 , GRCh38.p12 chr1: 170,790,859-174,760,863 FASLG, SERPINC1, 87 more genes
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