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Items: 1 to 20 of 1111

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148200copy number variation1nstd102humanUncertain significance GRCh37 chr22: 22,989,224-23,657,709 , GRCh38.p12 chr22: 22,646,754-23,315,522 IGLJ7, IGLC1, 66 more genes
    nsv7137145copy number variation1nstd102humanPathogenic GRCh37 chr22: 22,893,189-24,177,119 , GRCh38.p12 chr22: 22,550,767-23,834,932 CCDC188BP, DERL3, 99 more genes
    nsv7093384copy number variation1nstd102humanUncertain significance GRCh37 chr22: 22,988,816-23,657,709 , GRCh38.p12 chr22: 22,646,346-23,315,522 IGLC7, IGLV3-24, 66 more genes
    nsv7074576inversion1nstd229human GRCh38 chr22: 22,627,224-24,221,759 , GRCh37.p13 chr22: 22,969,695-24,617,727 IGLJ1, IGLV3-25, 107 more genes
    nsv7073094inversion1nstd229human GRCh38 chr22: 22,618,607-30,089,219 , GRCh37.p13 chr22: 22,961,077-30,485,208 BCRP1, POM121L10P, 237 more genes
    nsv7069551inversion1nstd229human GRCh38 chr22: 22,654,707-24,242,509 , GRCh37.p13 chr22: 22,997,177-24,638,477 IGLV3-27, MIF-AS1, 103 more genes
    nsv7061309inversion1nstd229human GRCh38 chr22: 22,581,345-23,017,946 , GRCh37.p13 chr22: 22,923,809-23,360,114 IGLV2-5, IGLV3-13, 62 more genes
    nsv7035422copy number variation1nstd229human GRCh38 chr22: 22,196,346-22,918,168 , GRCh37.p13 chr22: 22,550,746-23,260,340 IGLJ4, IGLV1-41, 98 more genes
    nsv7033383copy number variation1nstd229human GRCh38 chr22: 22,634,201-23,005,000 , GRCh37.p13 chr22: 22,976,672-23,347,167 IGLC5, IGLV3-29, 58 more genes
    nsv7025973copy number variation1nstd229human GRCh38 chr22: 22,793,002-22,893,780 , GRCh37.p13 chr22: 23,135,491-23,235,960 IGLJ1, IGLV2-11, 17 more genes
    nsv7024138copy number variation1nstd229human GRCh38 chr22: 22,887,583-22,895,182 , GRCh37.p13 chr22: 23,229,763-23,237,362 IGLL5, IGLC1, 2 more genes
    nsv7021644copy number variation1nstd229human GRCh38 chr22: 22,759,213-22,904,988 , GRCh37.p13 chr22: 23,101,702-23,247,168 IGLV3-7, IGLV3-12, 25 more genes
    nsv7021075copy number variation1nstd229human GRCh38 chr22: 22,772,588-22,893,787 , GRCh37.p13 chr22: 23,115,081-23,235,967 IGLV2-8, MIR5571, 19 more genes
    nsv7020199copy number variation1nstd229human GRCh38 chr22: 22,713,197-22,893,782 , GRCh37.p13 chr22: 23,055,682-23,235,962 IGLL5, LOC100420967, 28 more genes
    nsv7018593copy number variation1nstd229human GRCh38 chr22: 22,850,652-22,893,786 , GRCh37.p13 chr22: 23,192,827-23,235,966 IGLV3-2, LOC105372948, 11 more genes
    nsv7018183copy number variation1nstd229human GRCh38 chr22: 22,759,167-22,893,780 , GRCh37.p13 chr22: 23,101,656-23,235,960 LOC100420967, IGLV3-10, 21 more genes
    nsv6637777copy number variation1nstd102humanPathogenic GRCh37 chr22: 22,997,929-24,995,256 , GRCh38.p12 chr22: 22,655,459-24,599,289 LOC105372947, GGT5, 117 more genes
    nsv6637572copy number variation1nstd102humanLikely pathogenic GRCh37 chr22: 22,997,929-23,650,871 , GRCh38.p12 chr22: 22,655,459-23,308,684 BCR, GNAZ, 64 more genes
    nsv6637240copy number variation1nstd102humanLikely pathogenic GRCh37 chr22: 22,953,515-24,995,256 , GRCh38.p12 chr22: 22,611,045-24,599,289 ADORA2A, ASLP1, 122 more genes
    nsv6627193copy number variation1nstd224human GRCh37 chr22: 22,989,304-25,010,874 , GRCh38.p12 chr22: 22,646,834-24,614,907 GGT1, GNAZ, 119 more genes
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