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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7051174inversion1nstd229human GRCh38 chr2: 55,792,749-55,978,458 , GRCh37.p13 chr2: 56,019,884-56,205,593 EFEMP1, MIR217HG, 3 more genes
    nsv7050707inversion1nstd229human GRCh38 chr2: 49,559,122-58,358,849 , GRCh37.p13 chr2: 49,786,260-58,585,984 CDPF1P1, MIR3682, 86 more genes
    nsv7050246inversion1nstd229human GRCh38 chr2: 55,785,821-56,093,334 , GRCh37.p13 chr2: 56,012,956-56,320,469 MIR217, LINC01813, 7 more genes
    nsv7046688inversion1nstd229human GRCh38 chr2: 56,002,429-56,002,452 , GRCh37.p13 chr2: 56,229,564-56,229,587 LOC105374690, MIR217HG
    nsv6677893copy number variation1nstd229human GRCh38 chr2: 55,863,751-55,980,134 , GRCh37.p13 chr2: 56,090,886-56,207,269 EFEMP1, MIR217HG, 3 more genes
    nsv6677850copy number variation1nstd229human GRCh38 chr2: 56,024,474-56,265,758 , GRCh37.p13 chr2: 56,251,609-56,492,893 RNA5SP93, MIR217HG, 4 more genes
    nsv6676639copy number variation1nstd229human GRCh38 chr2: 56,038,001-56,076,600 , GRCh37.p13 chr2: 56,265,136-56,303,735 MIR217HG, LOC105374690, 1 more genes
    nsv6675687copy number variation1nstd229human GRCh38 chr2: 56,006,640-56,109,528 , GRCh37.p13 chr2: 56,233,775-56,336,663 MIR217HG, LOC105374690, 1 more genes
    nsv6674799copy number variation1nstd229human GRCh38 chr2: 56,017,301-56,024,100 , GRCh37.p13 chr2: 56,244,436-56,251,235 MIR217HG, LOC105374690
    nsv6674538copy number variation1nstd229human GRCh38 chr2: 56,034,958-56,035,101 , GRCh37.p13 chr2: 56,262,093-56,262,236 MIR217HG, LOC105374690
    nsv6673300copy number variation1nstd229human GRCh38 chr2: 56,038,801-56,047,100 , GRCh37.p13 chr2: 56,265,936-56,274,235 MIR217HG, LOC105374690
    nsv6672363copy number variation1nstd229human GRCh38 chr2: 55,997,064-55,997,609 , GRCh37.p13 chr2: 56,224,199-56,224,744 MIR217HG, LOC105374690
    nsv6667850copy number variation1nstd229human GRCh38 chr2: 55,691,620-56,076,078 , GRCh37.p13 chr2: 55,918,755-56,303,213 MIR217HG, EFEMP1, 9 more genes
    nsv6667398copy number variation1nstd229human GRCh38 chr2: 55,984,924-56,017,797 , GRCh37.p13 chr2: 56,212,059-56,244,932 MIR216B, MIR216A, 2 more genes
    nsv6666292copy number variation1nstd229human GRCh38 chr2: 55,923,219-55,992,441 , GRCh37.p13 chr2: 56,150,354-56,219,576 EFEMP1, MIR216A, 4 more genes
    nsv6664716copy number variation1nstd229human GRCh38 chr2: 56,033,496-56,037,124 , GRCh37.p13 chr2: 56,260,631-56,264,259 MIR217HG, LOC105374690
    nsv6661863copy number variation1nstd229human GRCh38 chr2: 56,002,277-56,002,459 , GRCh37.p13 chr2: 56,229,412-56,229,594 MIR217HG, LOC105374690
    nsv6659224copy number variation1nstd229human GRCh38 chr2: 55,991,978-55,992,048 , GRCh37.p13 chr2: 56,219,113-56,219,183 MIR217HG, LOC105374690
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6627893copy number variation1nstd224human GRCh37 chr2: 55,420,825-56,896,299 , GRCh38.p12 chr2: 55,193,689-56,669,164 RPS27A, PNPT1, 26 more genes
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