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Items: 1 to 20 of 275

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958899copy number variation1nstd209human GRCh38 chr22: 22,653,852-24,634,860 , GRCh37.p13 chr22: 22,996,322-25,030,827 , LOC105372957, 122 more genes
    nsv5956621copy number variation1nstd209human GRCh38 chr22: 22,621,614-24,637,144 , GRCh37.p13 chr22: 22,964,084-25,033,111 , IGLV2-5, 125 more genes
    nsv5885770copy number variation1nstd209human GRCh38 chr22: 23,429,495-23,432,099 , GRCh37.p13 chr22: 23,771,682-23,774,286 LINC01659
    nsv5709886mobile element insertion2nstd211human GRCh38 chr22: 23,434,164-23,434,164 , GRCh37.p13 chr22: 23,776,351-23,776,351 LINC01659
    nsv5414097mobile element insertion1nstd206human GRCh38 chr22: 23,434,164-23,434,215 , GRCh37.p13 chr22: 23,776,351-23,776,402 LINC01659
    nsv5381087copy number variation1nstd102humanPathogenic GRCh37 chr22: 23,699,269-24,992,266 , GRCh38.p12 chr22: 23,357,082-24,596,299 LOC100129358, VPREB3, 49 more genes
    nsv5291988copy number variation1nstd204human GRCh38.p13 chr22: 23,429,445-23,432,099 , GRCh37.p13 chr22: 23,771,632-23,774,286 LINC01659
    nsv5284835copy number variation1nstd204human GRCh38.p13 chr22: 23,430,901-23,432,300 , GRCh37.p13 chr22: 23,773,088-23,774,487 LINC01659
    nsv5163978mobile element insertion1nstd203human GRCh38 chr22: 23,434,152-23,434,164 , GRCh37.p13 chr22: 23,776,339-23,776,351 LINC01659
    nsv5036706copy number variation1nstd200human GRCh38 chr22: 23,254,265-23,655,581 , GRCh37.p13 chr22: 23,596,452-23,997,768 RPS10P30, LINC01659, 18 more genes
    nsv5035136copy number variation1nstd200human GRCh38 chr22: 23,257,914-23,477,063 , GRCh37.p13 chr22: 23,600,101-23,819,250 CCDC188BP, BCR, 10 more genes
    nsv5032403copy number variation1nstd200human GRCh38 chr22: 23,400,673-23,479,634 , GRCh37.p13 chr22: 23,742,860-23,821,821 FAM230I, LINC01659, 1 more genes
    nsv5029617copy number variation1nstd200human GRCh38 chr22: 23,263,396-23,657,194 , GRCh37.p13 chr22: 23,605,583-23,999,381 RPS10P30, LINC02556, 17 more genes
    nsv4869366copy number variation1nstd200human GRCh37 chr22: 23,600,101-23,819,250 , GRCh38.p12 chr22: 23,257,914-23,477,063 , GRCh38.p12 chr22|NT_187632.1: 1-123,021 RPS10P30, LINC01659, 10 more genes
    nsv4768383copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-26,483,608 , GRCh38.p12 chr22: 16,408,173-26,087,642 KRT18P62, LOC101060852, 437 more genes
    nsv4729959copy number variation1nstd102humanPathogenic GRCh37 chr22: 23,650,873-25,043,046 , GRCh38.p12 chr22: 23,308,686-24,647,079 BCRP1, SNRPD3, 55 more genes
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 FBXO7, GTSE1, 1084 more genes
    nsv4729872copy number variation1nstd102humanPathogenic GRCh37 chr22: 23,258,368-25,059,827 , GRCh38.p12 chr22: 22,916,198-24,663,860 LOC105372957, RAB36, 71 more genes
    nsv4729862copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,798,906-23,805,099 , GRCh38.p12 chr22: 21,444,617-23,462,912 LL22NC03-63E9.3, IGLC4, 158 more genes
    nsv4729784copy number variation1nstd102humanUncertain significance GRCh37 chr22: 23,720,181-25,066,484 , GRCh38.p12 chr22: 23,377,994-24,670,517 POM121L10P, GGTLC4P, 51 more genes
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