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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
    nsv7041253inversion1nstd229human GRCh38 chr1: 21,707,064-21,707,142 , GRCh37.p13 chr1: 22,033,557-22,033,635 USP48
    nsv6647258copy number variation1nstd229human GRCh38 chr1: 21,762,001-21,764,200 , GRCh37.p13 chr1: 22,088,494-22,090,693 USP48
    nsv6647257copy number variation1nstd229human GRCh38 chr1: 21,640,594-21,724,650 , GRCh37.p13 chr1: 21,967,087-22,051,143 USP48, 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
    nsv6647190copy number variation1nstd229human GRCh38 chr1: 21,766,898-21,770,702 , GRCh37.p13 chr1: 22,093,391-22,097,195 USP48
    nsv6647189copy number variation1nstd229human GRCh38 chr1: 21,763,870-21,769,810 , GRCh37.p13 chr1: 22,090,363-22,096,303 USP48
    nsv6647188copy number variation1nstd229human GRCh38 chr1: 21,746,968-21,747,087 , GRCh37.p13 chr1: 22,073,461-22,073,580 USP48
    nsv6647187copy number variation1nstd229human GRCh38 chr1: 21,685,842-21,685,919 , GRCh37.p13 chr1: 22,012,335-22,012,412 USP48
    nsv6646750copy number variation1nstd229human GRCh38 chr1: 21,783,628-21,830,305 , GRCh37.p13 chr1: 22,110,121-22,156,798 USP48, HSPG2, 1 more genes
    nsv6646747copy number variation1nstd229human GRCh38 chr1: 21,730,301-21,735,400 , GRCh37.p13 chr1: 22,056,794-22,061,893 USP48
    nsv6646745copy number variation1nstd229human GRCh38 chr1: 21,714,135-21,714,522 , GRCh37.p13 chr1: 22,040,628-22,041,015 USP48
    nsv6646744copy number variation1nstd229human GRCh38 chr1: 21,707,701-22,087,100 , GRCh37.p13 chr1: 22,034,194-22,413,593 LDLRAD2, HSPG2, 13 more genes
    nsv6552919inversion1nstd223human GRCh38 chr1: 21,774,986-21,775,110 , GRCh37.p13 chr1: 22,101,479-22,101,603 USP48
    nsv6551119inversion1nstd223human GRCh38 chr1: 21,767,077-21,767,530 , GRCh37.p13 chr1: 22,093,570-22,094,023 USP48
    nsv6546025inversion1nstd223human GRCh38 chr1: 21,731,265-21,731,886 , GRCh37.p13 chr1: 22,057,758-22,058,379 USP48
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