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Items: 1 to 20 of 126

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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
    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
    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
    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
    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
    nsv6626755copy number variation1nstd224human GRCh37 chr20: 23,419,556-23,567,918 , GRCh38.p12 chr20: 23,438,919-23,587,281 CST8, CSTL1, 6 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
    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
    nsv6251328mobile element insertion1nstd215human GRCh38 chr20: 23,438,281-23,438,281 , GRCh37.p13 chr20: 23,418,918-23,418,918 CSTL1
    nsv6134280copy number variation1nstd213human GRCh37 chr20: 22,530,000-23,650,001 , GRCh38.p12 chr20: 22,549,362-23,669,364 CST3, CYB5AP4, 33 more genes
    nsv6134279copy number variation1nstd213human GRCh37 chr20: 22,140,000-23,520,001 , GRCh38.p12 chr20: 22,159,362-23,539,364 RNA5SP478, LNCNEF, 34 more genes
    nsv6134275copy number variation1nstd213human GRCh37 chr20: 19,430,000-23,860,001 , GRCh38.p12 chr20: 19,449,356-23,879,364 CST1, CST4, 87 more genes
    nsv6133908copy number variation1nstd213human GRCh37 chr20: 23,010,000-23,580,001 , GRCh38.p12 chr20: 23,029,363-23,599,364 SSTR4, THBD, 20 more genes
    nsv5698757mobile element insertion1nstd211human GRCh38 chr20: 23,438,281-23,438,281 , GRCh37.p13 chr20: 23,418,918-23,418,918 CSTL1
    nsv5527137copy number variation1nstd206human GRCh38 chr20: 23,428,335-23,589,000 , GRCh37.p13 chr20: 23,408,972-23,569,637 CST8, CSTL1, 6 more genes
    nsv5432011mobile element insertion1nstd206human GRCh38 chr20: 23,438,281-23,438,332 , GRCh37.p13 chr20: 23,418,918-23,418,969 CSTL1
    nsv5025212copy number variation1nstd200human GRCh38 chr20: 23,437,226-23,447,701 , GRCh37.p13 chr20: 23,417,863-23,428,338 CSTL1
    nsv4729864copy number variation1nstd102humanLikely benign GRCh37 chr20: 23,413,239-23,569,271 , GRCh38.p12 chr20: 23,432,602-23,588,634 CST8, CSTL1, 6 more genes
    nsv4729757copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 19,750,804-30,479,077 , GRCh38.p12 chr20: 19,770,160-31,891,274 BCL2L1, CD24P3, 222 more genes
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