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Items: 1 to 20 of 213

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145215insertion1nstd232human GRCh37.p13 chr1: 150,691,450-150,691,450 , GRCh38.p12 chr1: 150,718,974-150,718,974 HORMAD1
    nsv7099231copy number variation1nstd231human GRCh38.p12 chr1: 149,962,894-151,006,586 , GRCh37 chr1: 149,934,818-150,979,062 ARNT, CTSK, 48 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
    nsv6641929copy number variation1nstd229human GRCh38 chr1: 150,718,975-150,719,310 , GRCh37.p13 chr1: 150,691,451-150,691,786 HORMAD1
    nsv6641916copy number variation1nstd229human GRCh38 chr1: 150,406,738-150,700,622 , GRCh37.p13 chr1: 150,440,214-150,673,098 RNU6-1042P, ENSA, 16 more genes
    nsv6641678copy number variation1nstd229human GRCh38 chr1: 150,721,401-150,736,047 , GRCh37.p13 chr1: 150,693,877-150,708,523 HORMAD1, CTSS
    nsv6641677copy number variation1nstd229human GRCh38 chr1: 150,699,524-150,702,999 , GRCh37.p13 chr1: 150,672,000-150,675,475 HORMAD1, RNU6-1042P
    nsv6641676copy number variation1nstd229human GRCh38 chr1: 150,688,738-150,697,155 , GRCh37.p13 chr1: 150,661,214-150,669,631 GOLPH3L, HORMAD1
    nsv6325277copy number variation1nstd223human GRCh38 chr1: 150,699,524-150,702,996 , GRCh37.p13 chr1: 150,672,000-150,675,472 HORMAD1, RNU6-1042P
    nsv6325017copy number variation1nstd223human GRCh38 chr1: 150,718,975-150,719,293 , GRCh37.p13 chr1: 150,691,451-150,691,769 HORMAD1
    nsv6322289copy number variation1nstd223human GRCh38 chr1: 150,721,401-150,736,010 , GRCh37.p13 chr1: 150,693,877-150,708,486 CTSS, HORMAD1
    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
    nsv6245257mobile element insertion1nstd215human GRCh38 chr1: 150,713,404-150,713,404 , GRCh37.p13 chr1: 150,685,880-150,685,880 HORMAD1
    nsv6245256mobile element insertion1nstd215human GRCh38 chr1: 150,698,166-150,698,166 , GRCh37.p13 chr1: 150,670,642-150,670,642 HORMAD1
    nsv6133734copy number variation1nstd213human GRCh37 chr1: 150,350,000-154,440,001 , GRCh38.p12 chr1: 150,377,524-154,467,525 , MCL1, 216 more genes
    nsv6133733copy number variation1nstd213human GRCh37 chr1: 149,980,000-151,620,001 , GRCh38.p12 chr1: 150,008,051-151,647,525 CTSK, MCL1, 80 more genes
    nsv6133732copy number variation1nstd213human GRCh37 chr1: 149,750,000-153,310,001 , GRCh38.p12 chr1: 149,778,444-153,337,525 , CTSK, 183 more genes
    nsv6133499copy number variation1nstd213human GRCh37 chr1: 149,880,000-153,720,001 , GRCh38.p12 chr1: 149,908,448-153,747,525 , CTSK, 198 more genes
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