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Items: 1 to 20 of 271

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099184copy number variation1nstd231human GRCh38.p12 chr1: 21,486,574-23,087,716 , GRCh37 chr1: 21,813,067-23,414,209 ALPL, C1QA, 36 more genes
    nsv7095949copy number variation1nstd102humanUncertain significance GRCh37 chr1: 19,199,339-24,690,861 , GRCh38.p12 chr1: 18,872,845-24,364,371 RPL29P6, NBPF3, 156 more genes
    nsv7095496copy number variation3nstd102humanUncertain significance GRCh37 chr1: 19,199,339-22,987,879 , GRCh38.p12 chr1: 18,872,845-22,661,386 RN7SL277P, MPHOSPH6P1, 103 more genes
    nsv7055295inversion1nstd229human GRCh38 chr1: 20,526,331-21,860,622 , GRCh37.p13 chr1: 20,852,824-22,187,115 USP48, ECE1, 31 more genes
    nsv7051148inversion1nstd229human GRCh38 chr1: 21,508,157-21,619,903 , GRCh37.p13 chr1: 21,834,650-21,946,396 RAP1GAP, LINC02596, 1 more genes
    nsv6647257copy number variation1nstd229human GRCh38 chr1: 21,640,594-21,724,650 , GRCh37.p13 chr1: 21,967,087-22,051,143 USP48, RAP1GAP
    nsv6647256copy number variation1nstd229human GRCh38 chr1: 21,630,104-21,634,505 , GRCh37.p13 chr1: 21,956,597-21,960,998 RAP1GAP
    nsv6647254copy number variation1nstd229human GRCh38 chr1: 21,562,611-27,513,090 , GRCh37.p13 chr1: 21,889,104-27,839,601 RPL18AP5, LINC00339, 184 more genes
    nsv6647227copy number variation1nstd229human GRCh38 chr1: 20,848,934-27,947,465 , GRCh37.p13 chr1: 21,175,427-28,273,976 RPL17P9, ALPL, 218 more genes
    nsv6647186copy number variation1nstd229human GRCh38 chr1: 21,648,697-21,651,734 , GRCh37.p13 chr1: 21,975,190-21,978,227 RAP1GAP
    nsv6647185copy number variation1nstd229human GRCh38 chr1: 21,634,971-21,640,992 , GRCh37.p13 chr1: 21,961,464-21,967,485 RAP1GAP
    nsv6647184copy number variation1nstd229human GRCh38 chr1: 21,564,401-21,607,800 , GRCh37.p13 chr1: 21,890,894-21,934,293 ALPL, RAP1GAP, 1 more genes
    nsv6647128copy number variation1nstd229human GRCh38 chr1: 21,653,389-21,656,653 , GRCh37.p13 chr1: 21,979,882-21,983,146 RAP1GAP
    nsv6647127copy number variation1nstd229human GRCh38 chr1: 21,640,073-21,643,871 , GRCh37.p13 chr1: 21,966,566-21,970,364 RAP1GAP
    nsv6647126copy number variation1nstd229human GRCh38 chr1: 21,626,777-21,636,270 , GRCh37.p13 chr1: 21,953,270-21,962,763 RAP1GAP
    nsv6647124copy number variation1nstd229human GRCh38 chr1: 21,542,001-21,659,500 , GRCh37.p13 chr1: 21,868,494-21,985,993 LINC02596, ALPL, 1 more genes
    nsv6646742copy number variation1nstd229human GRCh38 chr1: 21,624,429-21,639,904 , GRCh37.p13 chr1: 21,950,922-21,966,397 RAP1GAP
    nsv6646741copy number variation1nstd229human GRCh38 chr1: 21,623,494-21,627,548 , GRCh37.p13 chr1: 21,949,987-21,954,041 RAP1GAP
    nsv6332841copy number variation1nstd223human GRCh38 chr1: 21,648,701-21,652,000 , GRCh37.p13 chr1: 21,975,194-21,978,493 RAP1GAP
    nsv6328488copy number variation1nstd223human GRCh38 chr1: 21,618,301-21,619,500 , GRCh37.p13 chr1: 21,944,794-21,945,993 RAP1GAP
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