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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099232copy number variation1nstd231human GRCh38.p12 chr1: 151,364,317-152,231,192 , GRCh37 chr1: 151,336,793-152,203,668 , PSMB4, 37 more genes
    nsv7056211inversion1nstd229human GRCh38 chr1: 143,881,700-152,159,818 , GRCh37.p13 chr1|NW_003871055.3: 697,113-7,283,150 , PDIA3P1, 333 more genes
    nsv7044458inversion1nstd229human GRCh38 chr1: 150,355,899-155,246,175 , GRCh37.p13 chr1: 150,440,214-155,215,966 LCE2C, MUC1, 254 more genes
    nsv7042502inversion1nstd229human GRCh38 chr1: 150,301,267-155,517,761 , GRCh37.p13 chr1: 150,440,214-155,487,552 LINGO4, CELF3, 268 more genes
    nsv6625842copy number variation1nstd224human GRCh37 chr1: 151,337,703-151,411,444 , GRCh38.p12 chr1: 151,365,227-151,438,968 SELENBP1, POGZ, 2 more genes
    nsv6625841copy number variation8nstd224human GRCh37 chr1: 151,337,060-151,407,693 , GRCh38.p12 chr1: 151,364,584-151,435,217 PSMB4, SELENBP1, 1 more genes
    nsv6625771copy number variation1nstd224human GRCh37 chr1: 151,340,680-151,407,693 , GRCh38.p12 chr1: 151,368,204-151,435,217 PSMB4, SELENBP1, 1 more genes
    nsv6625770copy number variation1nstd224human GRCh37 chr1: 151,337,690-151,407,693 , GRCh38.p12 chr1: 151,365,214-151,435,217 SELENBP1, POGZ, 1 more genes
    nsv6625644copy number variation1nstd224human GRCh37 chr1: 151,341,499-151,407,693 , GRCh38.p12 chr1: 151,369,023-151,435,217 SELENBP1, POGZ, 1 more genes
    nsv6625643copy number variation1nstd224human GRCh37 chr1: 151,337,703-151,407,693 , GRCh38.p12 chr1: 151,365,227-151,435,217 POGZ, SELENBP1, 1 more genes
    nsv6625642copy number variation6nstd224human GRCh37 chr1: 151,337,703-151,397,884 , GRCh38.p12 chr1: 151,365,227-151,425,408 SELENBP1, POGZ, 1 more genes
    nsv6625400copy number variation1nstd224human GRCh37 chr1: 151,372,047-151,386,471 , GRCh38.p12 chr1: 151,399,571-151,413,995 PSMB4, POGZ
    nsv6625399copy number variation3nstd224human GRCh37 chr1: 151,340,675-151,407,693 , GRCh38.p12 chr1: 151,368,199-151,435,217 PSMB4, SELENBP1, 1 more genes
    nsv6625398copy number variation1nstd224human GRCh37 chr1: 151,339,307-151,407,693 , GRCh38.p12 chr1: 151,366,831-151,435,217 PSMB4, SELENBP1, 1 more genes
    nsv6625397copy number variation2nstd224human GRCh37 chr1: 151,339,231-151,407,693 , GRCh38.p12 chr1: 151,366,755-151,435,217 PSMB4, SELENBP1, 1 more genes
    nsv6625396copy number variation1nstd224human GRCh37 chr1: 151,338,753-151,407,693 , GRCh38.p12 chr1: 151,366,277-151,435,217 SELENBP1, POGZ, 1 more genes
    nsv6315165copy number variation1nstd102humanPathogenic GRCh37 chr1: 151,372,064-151,384,872 , GRCh38.p12 chr1: 151,399,588-151,412,396 PSMB4, POGZ
    nsv6310726copy number variation1nstd102humanUncertain significance GRCh37 chr1: 151,372,055-151,374,305 , GRCh38.p12 chr1: 151,399,579-151,401,829 POGZ, PSMB4
    nsv6310678copy number variation4nstd102humanUncertain significance GRCh37 chr1: 149,895,434-156,851,434 , GRCh38.p12 chr1: 149,923,542-156,881,642 PRPF3, KHDC4, 352 more genes
    nsv6138677copy number variation1nstd206human GRCh38 chr1: 151,359,540-151,436,045 , GRCh37.p13 chr1: 151,332,016-151,408,521 SELENBP1, POGZ, 1 more genes
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