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Items: 1 to 20 of 168

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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
    nsv7143721insertion1nstd232human GRCh37.p13 chr20: 23,614,637-23,614,637 , GRCh38.p12 chr20: 23,634,000-23,634,000 CST3
    nsv7137993copy number variation1nstd232human GRCh37.p13 chr20: 23,605,491-23,605,562 , GRCh38.p12 chr20: 23,624,854-23,624,925 CST3
    nsv7060339inversion1nstd229human GRCh38 chr20: 23,599,888-23,883,729 , GRCh37.p13 chr20: 23,580,525-23,864,366 CST9, CST1, 9 more genes
    nsv7035921copy number variation1nstd229human GRCh38 chr20: 23,407,997-23,871,822 , GRCh37.p13 chr20: 23,388,634-23,852,459 CST12P, CST8, 17 more genes
    nsv7034471copy number variation1nstd229human GRCh38 chr20: 23,625,717-23,627,691 , GRCh37.p13 chr20: 23,606,354-23,608,328 CST3
    nsv7032175copy number variation1nstd229human GRCh38 chr20: 23,493,451-23,727,872 , GRCh37.p13 chr20: 23,474,088-23,708,509 LOC107985383, CST4, 8 more genes
    nsv7032011copy number variation1nstd229human GRCh38 chr20: 23,203,457-24,359,303 , GRCh37.p13 chr20: 23,184,094-24,339,939 CST9, RNU1-23P, 32 more genes
    nsv7029901copy number variation1nstd229human GRCh38 chr20: 23,522,540-24,257,872 , GRCh37.p13 chr20: 23,503,177-24,238,508 POM121L3P, CST4, 20 more genes
    nsv7022644copy number variation1nstd229human GRCh38 chr20: 23,635,369-23,637,619 , GRCh37.p13 chr20: 23,616,006-23,618,256 CST3
    nsv7020679copy number variation1nstd229human GRCh38 chr20: 23,393,385-24,073,730 , GRCh37.p13 chr20: 23,374,022-24,054,367 LOC107985438, CSTP2, 22 more genes
    nsv7020509copy number variation1nstd229human GRCh38 chr20: 23,615,882-23,628,999 , GRCh37.p13 chr20: 23,596,519-23,609,636 CST3
    nsv7019162copy number variation1nstd229human GRCh38 chr20: 23,615,001-23,627,800 , GRCh37.p13 chr20: 23,595,638-23,608,437 CST3
    nsv7019012copy number variation1nstd229human GRCh38 chr20: 23,628,201-23,629,900 , GRCh37.p13 chr20: 23,608,838-23,610,537 CST3
    nsv6637732copy number variation1nstd102humanUncertain significance GRCh37 chr20: 23,142,478-24,824,349 , GRCh38.p12 chr20: 23,161,841-24,843,713 NAPB, POM121L3P, 37 more genes
    nsv6626754copy number variation1nstd224human GRCh37 chr20: 23,375,624-24,052,857 , GRCh38.p12 chr20: 23,394,987-24,072,220 CST5, GGTLC1, 22 more genes
    nsv6626753copy number variation1nstd224human GRCh37 chr20: 23,369,317-24,042,329 , GRCh38.p12 chr20: 23,388,680-24,061,692 CST3, CSTP2, 22 more genes
    nsv6626551copy number variation1nstd224human GRCh37 chr20: 23,594,292-23,860,259 , GRCh38.p12 chr20: 23,613,655-23,879,622 CST1, CST4, 8 more genes
    nsv6524309copy number variation1nstd223human GRCh38 chr20: 23,628,222-23,629,920 , GRCh37.p13 chr20: 23,608,859-23,610,557 CST3
    nsv6291578copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413 AHCY, ASIP, 330 more genes
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