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Items: 1 to 20 of 219

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148056copy number variation1nstd102humanPathogenic GRCh37 chr2: 186,698,504-223,918,111 , GRCh38.p12 chr2: 185,833,777-223,053,393 DNAJB1P1, MTCO2P17, 580 more genes
    nsv6684916copy number variation1nstd229human GRCh38 chr2: 202,876,655-202,880,051 , GRCh37.p13 chr2: 203,741,378-203,744,774 WDR12
    nsv6683634copy number variation1nstd229human GRCh38 chr2: 202,896,501-202,979,100 , GRCh37.p13 chr2: 203,761,224-203,843,823 WDR12, KRT8P52, 1 more genes
    nsv6678126copy number variation1nstd229human GRCh38 chr2: 202,769,401-202,924,400 , GRCh37.p13 chr2: 203,634,124-203,789,123 WDR12, LOC442064, 5 more genes
    nsv6637127copy number variation1nstd102humanPathogenic GRCh37 chr2: 189,909,904-209,468,383 , GRCh38.p12 chr2: 189,045,178-208,603,658 LOC100421409, LOC100507443, 310 more genes
    nsv6552889inversion1nstd223human GRCh38 chr2: 202,879,687-202,880,354 , GRCh37.p13 chr2: 203,744,410-203,745,077 WDR12
    nsv6542155inversion1nstd223human GRCh38 chr2: 202,897,662-202,898,157 , GRCh37.p13 chr2: 203,762,385-203,762,880 WDR12
    nsv6541862inversion1nstd223human GRCh38 chr2: 202,895,704-202,896,418 , GRCh37.p13 chr2: 203,760,427-203,761,141 WDR12
    nsv6541724inversion1nstd223human GRCh38 chr2: 202,909,828-202,910,506 , GRCh37.p13 chr2: 203,774,551-203,775,229 CARF, WDR12
    nsv6537016inversion1nstd223human GRCh38 chr2: 202,886,477-202,887,333 , GRCh37.p13 chr2: 203,751,200-203,752,056 WDR12
    nsv6351180copy number variation1nstd223human GRCh38 chr2: 202,892,201-202,894,000 , GRCh37.p13 chr2: 203,756,924-203,758,723 WDR12
    nsv6345782copy number variation1nstd223human GRCh38 chr2: 202,872,773-202,879,988 , GRCh37.p13 chr2: 203,737,496-203,744,711 WDR12
    nsv6341796copy number variation1nstd223human GRCh38 chr2: 202,878,046-202,879,286 , GRCh37.p13 chr2: 203,742,769-203,744,009 WDR12
    nsv6339532copy number variation1nstd223human GRCh38 chr2: 202,896,832-202,897,734 , GRCh37.p13 chr2: 203,761,555-203,762,457 WDR12
    nsv6336346copy number variation1nstd223human GRCh38 chr2: 202,867,801-202,874,300 , GRCh37.p13 chr2: 203,732,524-203,739,023 ICA1L, WDR12
    nsv6315398copy number variation1nstd102humanPathogenic GRCh37 chr2: 185,697,659-213,002,074 , GRCh38.p12 chr2: 184,832,932-212,137,349 LOC107985785, MYO1B, 381 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313730copy number variation1nstd102humanPathogenic GRCh37 chr2: 200,851,079-209,054,267 , GRCh38.p12 chr2: 199,986,356-208,189,543 RN7SKP200, PIMREGP1, 179 more genes
    nsv6311631copy number variation1nstd102humanUncertain significance GRCh37 chr2: 203,420,070-211,811,277 , GRCh38.p12 chr2: 202,555,347-210,946,553 MIR3130-2, WDR12, 133 more genes
    nsv6311365copy number variation5nstd102humanUncertain significance, Pathogenic GRCh37 chr2: 201,943,606-204,824,322 , GRCh38.p12 chr2: 201,078,883-203,959,599 MTND4LP17, SNORD11, 87 more genes
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