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Items: 1 to 20 of 185

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148267copy number variation1nstd102humanPathogenic GRCh38 chr20: 87,153-23,635,465 , GRCh37.p13 chr20: 67,794-23,616,102 KRT18P3, RSPO4, 413 more genes
    nsv7096013copy number variation1nstd102humanPathogenic GRCh37 chr20: 10,653,329-10,654,278 , GRCh38.p12 chr20: 10,672,681-10,673,630 JAG1
    nsv7073551inversion1nstd229human GRCh38 chr20: 10,362,744-19,023,342 , GRCh37.p13 chr20: 10,343,392-19,003,986 SLX4IP, RPL15P1, 122 more genes
    nsv7036487copy number variation1nstd229human GRCh38 chr20: 10,449,828-13,745,757 , GRCh37.p13 chr20: 10,430,476-13,726,404 RN7SKP111, MIR6870, 36 more genes
    nsv7034574copy number variation1nstd229human GRCh38 chr20: 10,653,965-10,653,988 , GRCh37.p13 chr20: 10,634,613-10,634,636 JAG1
    nsv7022067copy number variation1nstd229human GRCh38 chr20: 7,868,752-11,491,709 , GRCh37.p13 chr20: 7,849,399-11,472,357 LOC339593, LOC105372522, 36 more genes
    nsv7020571copy number variation1nstd229human GRCh38 chr20: 10,636,401-10,642,600 , GRCh37.p13 chr20: 10,617,049-10,623,248 JAG1
    nsv6626488copy number variation1nstd224human GRCh37 chr20: 10,601,964-10,619,014 , GRCh38.p12 chr20: 10,621,316-10,638,366 JAG1, SLX4IP
    nsv6599358inversion1nstd223human GRCh38 chr20: 10,362,749-19,023,339 , GRCh37.p13 chr20: 10,343,397-19,003,983 JAG1, BFSP1, 122 more genes
    nsv6315526copy number variation1nstd102humanPathogenic GRCh37 chr20: 3,178,539-11,848,383 , GRCh38.p12 chr20: 3,197,893-11,867,735 LRRN4, MCM8-AS1, 129 more genes
    nsv6314184copy number variation1nstd102humanUncertain significance GRCh37 chr20: 10,573,642-10,778,864 , GRCh38.p12 chr20: 10,592,994-10,798,216 JAG1, LOC100421490, 4 more genes
    nsv6314112copy number variation1nstd102humanUncertain significance GRCh37 chr20: 10,522,024-10,627,551 , GRCh38.p12 chr20: 10,541,376-10,646,903 LOC100421490, SLX4IP, 1 more genes
    nsv6311245copy number variation1nstd102humanUncertain significance GRCh37 chr20: 7,812,350-10,654,278 , GRCh38.p12 chr20: 7,831,703-10,673,630 LOC100421490, RNU105B, 27 more genes
    nsv6311076copy number variation1nstd102humanUncertain significance GRCh37 chr20: 10,256,140-10,654,178 , GRCh38.p12 chr20: 10,275,492-10,673,530 MIR6870, SNAP25, 7 more genes
    nsv6133897copy number variation1nstd213human GRCh37 chr20: 10,470,000-10,660,001 , GRCh38.p12 chr20: 10,489,352-10,679,353 JAG1, SLX4IP, 2 more genes
    nsv6133808copy number variation1nstd213human GRCh37 chr20: 3,300,000-12,130,001 , GRCh38.p12 chr20: 3,319,353-12,149,353 BMP2, CDC25B, 126 more genes
    nsv6133792copy number variation1nstd213human GRCh37 chr20: 10,380,000-13,180,001 , GRCh38.p12 chr20: 10,399,352-13,199,354 JAG1, MKKS, 32 more genes
    nsv5381139copy number variation1nstd102humanUncertain significance GRCh37 chr20: 10,579,323-11,009,878 , GRCh38.p12 chr20: 10,598,675-11,029,230 LOC107985398, MIR6870, 7 more genes
    nsv5294962copy number variation1nstd204human GRCh38.p13 chr20: 10,669,401-10,673,200 , GRCh37.p13 chr20: 10,650,049-10,653,848 JAG1
    nsv5174624mobile element insertion1nstd203human GRCh38 chr20: 10,669,547-10,669,588 , GRCh37.p13 chr20: 10,650,195-10,650,236 JAG1
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