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Items: 1 to 20 of 237

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148251copy number variation1nstd102humanPathogenic GRCh38 chr3: 197,681,032-198,111,976 , GRCh37.p13 chr3: 197,407,903-197,838,847 RNU6-621P, RPL35A, 12 more genes
    nsv7098781copy number variation1nstd102humanUncertain significance GRCh37 chr3: 195,591,052-197,682,644 , GRCh38.p12 chr3: 195,864,181-197,955,773 ZDHHC19, DLG1, 68 more genes
    nsv7096709copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 197,680,864-197,682,644 , GRCh38.p12 chr3: 197,953,993-197,955,773 RPL35A, IQCG
    nsv7051130inversion1nstd229human GRCh38 chr3: 196,923,427-197,979,595 , GRCh37.p13 chr3: 196,650,298-197,706,466 LOC105374310, LINC02012, 29 more genes
    nsv7045657inversion1nstd229human GRCh38 chr3: 197,892,796-198,051,278 , GRCh37.p13 chr3: 197,619,667-197,778,149 IQCG, LMLN, 4 more genes
    nsv6737311copy number variation1nstd229human GRCh38 chr3: 197,864,734-198,006,922 , GRCh37.p13 chr3: 197,591,605-197,733,793 RPL35A, RNU6-858P, 4 more genes
    nsv6735491copy number variation1nstd229human GRCh38 chr3: 197,879,544-198,071,808 , GRCh37.p13 chr3: 197,606,415-197,798,679 IQCG, LMLN-AS1, 7 more genes
    nsv6734989copy number variation1nstd229human GRCh38 chr3: 197,839,176-198,108,692 , GRCh37.p13 chr3: 197,566,047-197,835,563 LOC105374310, RPL35A, 10 more genes
    nsv6733536copy number variation1nstd229human GRCh38 chr3: 197,918,404-198,026,036 , GRCh37.p13 chr3: 197,645,275-197,752,907 RPL35A, IQCG, 2 more genes
    nsv6733307copy number variation1nstd229human GRCh38 chr3: 197,396,684-198,059,614 , GRCh37.p13 chr3: 197,123,555-197,786,485 IQCG, LMLN-AS1, 19 more genes
    nsv6731402copy number variation1nstd229human GRCh38 chr3: 197,838,183-198,062,058 , GRCh37.p13 chr3: 197,565,054-197,788,929 RPL17P18, RNU6-858P, 8 more genes
    nsv6730698copy number variation1nstd229human GRCh38 chr3: 197,879,913-198,017,686 , GRCh37.p13 chr3: 197,606,784-197,744,557 LRCH3, RNU6-621P, 4 more genes
    nsv6729710copy number variation1nstd229human GRCh38 chr3: 197,836,096-197,959,141 , GRCh37.p13 chr3: 197,562,967-197,686,012 LMLN, IQCG, 5 more genes
    nsv6728277copy number variation1nstd229human GRCh38 chr3: 197,898,149-197,983,229 , GRCh37.p13 chr3: 197,625,020-197,710,100 IQCG, LMLN, 1 more genes
    nsv6720064copy number variation1nstd229human GRCh38 chr3: 197,394,307-197,957,911 , GRCh37.p13 chr3: 197,121,178-197,684,782 FYTTD1, RNU6-858P, 15 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6628942copy number variation1nstd224human GRCh37 chr3: 197,593,036-197,833,758 , GRCh38.p12 chr3: 197,866,165-198,106,887 RPL35A, IQCG, 7 more genes
    nsv6628562copy number variation1nstd224human GRCh37 chr3: 197,598,247-197,701,913 , GRCh38.p12 chr3: 197,871,376-197,975,042 RPL35A, LMLN, 3 more genes
    nsv6628561copy number variation2nstd224human GRCh37 chr3: 197,574,789-197,833,758 , GRCh38.p12 chr3: 197,847,918-198,106,887 RNU6-621P, RPL35A, 9 more genes
    nsv6628509copy number variation1nstd224human GRCh37 chr3: 197,670,652-197,835,115 , GRCh38.p12 chr3: 197,943,781-198,108,244 RPL35A, IQCG, 6 more genes
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