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Items: 1 to 20 of 287

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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
    nsv7070289inversion1nstd229human GRCh38 chr22: 23,101,987-23,504,319 , GRCh37.p13 chr22: 23,444,174-23,846,506 LINC02556, FBXW4P1, 15 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
    nsv7068518inversion1nstd229human GRCh38 chr22: 22,967,696-24,261,827 , GRCh37.p13 chr22: 23,309,870-24,657,795 DDT, POM121L11P, 51 more genes
    nsv7033738copy number variation1nstd229human GRCh38 chr22: 23,257,914-23,477,063 , GRCh37.p13 chr22: 23,600,101-23,819,250 RN7SL263P, RPS10P30, 10 more genes
    nsv7028873copy number variation1nstd229human GRCh38 chr22: 22,977,123-28,064,565 , GRCh37.p13 chr22: 23,319,297-28,460,553 LOC100652871, VPREB3, 132 more genes
    nsv7027438copy number variation1nstd229human GRCh38 chr22: 23,254,265-23,655,581 , GRCh37.p13 chr22: 23,596,452-23,997,768 ZDHHC8BP, LOC107985554, 18 more genes
    nsv7025124copy number variation1nstd229human GRCh38 chr22: 23,230,887-23,271,928 , GRCh37.p13 chr22: 23,573,074-23,614,115 RN7SL263P, FBXW4P1, 1 more genes
    nsv7021927copy number variation1nstd229human GRCh38 chr22: 23,262,067-23,262,088 , GRCh37.p13 chr22: 23,604,254-23,604,275 FBXW4P1, BCR, 1 more genes
    nsv7019702copy number variation1nstd229human GRCh38 chr22: 23,258,639-23,535,313 , GRCh37.p13 chr22: 23,600,826-23,877,500 CES5AP1, LOC107985554, 12 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
    nsv6627194copy number variation1nstd224human GRCh37 chr22: 23,600,013-23,996,463 , GRCh38.p12 chr22: 23,257,826-23,654,276 FBXW4P1, LINC02556, 18 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
    nsv6627184copy number variation1nstd224human GRCh37 chr22: 21,799,719-23,803,722 , GRCh38.p12 chr22: 21,445,430-23,461,535 BCRP4, GNAZ, 158 more genes
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