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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5665203inversion1nstd207human GRCh38 chr2: 113,578,563-113,598,318 , GRCh37.p13 chr2: 114,336,140-114,355,895 DDX11L2, WASH2P, 2 more genes
    nsv5558142mobile element insertion1nstd206human GRCh38 chr2: 102,295,972-141,288,199 , GRCh37.p13 chr2: 102,912,432-142,045,768 , LOC105373587, 623 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5442742copy number variation1nstd206human GRCh38 chr2: 113,233,158-113,804,713 , GRCh37.p13 chr2: 113,990,735-114,562,290 , SLC35F5, 22 more genes
    nsv5288343copy number variation1nstd204human GRCh38.p13 chr2: 113,322,640-114,227,007 , GRCh37.p13 chr2: 114,080,217-114,984,584 , FOXD4L1, 24 more genes
    nsv5206338copy number variation1nstd204human GRCh38.p13 chr2: 113,574,601-113,576,500 , GRCh37.p13 chr2: 114,332,178-114,334,077 FAM138B
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv5033955inversion1nstd200human GRCh38 chr2: 103,800,446-187,202,765 , GRCh37.p13 chr2: 104,416,904-188,067,492 , EDDM3CP, 1184 more genes
    nsv4879764inversion1nstd200human GRCh37 chr2: 104,416,904-188,067,492 , GRCh38.p12 chr2: 103,800,446-187,202,765 , ACMSD, 1184 more genes
    nsv4781720copy number variation1nstd200human GRCh37 chr2: 114,080,222-114,984,575 , GRCh38.p12 chr2: 113,322,645-114,226,998 , LOC105373567, 24 more genes
    nsv4743379copy number variation1nstd199human GRCh37 chr2: 88,481,090-124,440,189 , GRCh38.p12 chr9: 40,649,751-63,450,622 , GRCh38.p12 chr9: 40,649,907-63,450,751 , GRCh38.p12 chr1: 125,085,511-144,884,066 , GRCh38.p12 chr2: 88,181,571-123,682,613 , EIF2AK3, 861 more genes
    nsv4594867copy number variation1nstd183human GRCh37 chr2: 114,323,203-114,374,714 , GRCh38.p12 chr2: 113,565,626-113,617,137 DDX11L2, RPL23AP7, 4 more genes
    nsv4594866copy number variation1nstd183human GRCh37 chr2: 114,315,913-114,340,715 , GRCh38.p12 chr2: 113,558,336-113,583,138 WASH2P, MIR1302-3, 2 more genes
    nsv4583353copy number variation1nstd183human GRCh37 chr2: 114,236,536-114,337,894 , GRCh38.p12 chr2: 113,478,959-113,580,317 , ZNG1B, 5 more genes
    nsv4582169copy number variation2nstd183human GRCh37 chr2: 114,198,227-114,338,077 , GRCh38.p12 chr2: 113,440,650-113,580,500 , ZNG1B, 5 more genes
    nsv4409455copy number variation1nstd174human GRCh37 chr2: 114,322,271-114,376,565 , GRCh38.p12 chr2: 113,564,694-113,618,988 DDX11L2, RPL23AP7, 4 more genes
    nsv4401841copy number variation1nstd174human GRCh37 chr2: 114,310,836-114,337,313 , GRCh38.p12 chr2: 113,553,259-113,579,736 FAM138B, PGM5P4
    nsv4398683copy number variation1nstd174human GRCh37 chr2: 114,335,055-114,350,400 , GRCh38.p12 chr2: 113,577,478-113,592,823 WASH2P, MIR1302-3, 1 more genes
    nsv3923963copy number variation1nstd102humanUncertain significance NCBI36 chr2: 110,190,938-242,751,149 , GRCh37.p13 chr2: 110,833,649-243,102,476 , GRCh38.p12 chr2: 110,076,072-242,160,331 NMTRQ-TTG9-1, MIR6810, 1944 more genes
    nsv3921207copy number variation1nstd102humanPathogenic NCBI36 chr2: 110,857,227-116,449,787 , GRCh37.p13 chr2: 111,334,455-116,733,317 , GRCh38.p12 chr2: 110,576,878-115,975,741 RABL2A, RPL34P8, 98 more genes
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