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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112800copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,889,977-21,463,189 , GRCh38.p12 chr22: 18,339,130-21,108,900 MIR4761, TUBA3FP, 124 more genes
    nsv6112793copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,889,693-21,465,485 , GRCh38.p12 chr22: 18,339,130-21,111,196 THAP7, LOC100129262, 125 more genes
    nsv6112789copy number variation1nstd102humanPathogenic GRCh37 chr22: 20,730,996-21,465,342 , GRCh38.p12 chr22: 20,376,706-21,111,053 IGLL4P, CRKL, 39 more genes
    nsv6112781copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,841,374-21,465,101 , GRCh38.p12 chr22: 18,339,130-21,110,812 SEPTIN5, RNU6-225P, 125 more genes
    nsv6112779copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,889,571-21,464,697 , GRCh38.p12 chr22: 18,339,130-21,110,408 PRODH, MIR3618, 124 more genes
    nsv5980456copy number variation1nstd102humanUncertain significance GRCh37 chr22: 20,737,912-21,465,659 , GRCh38.p12 chr22: 20,383,622-21,111,370 KRT18P5, SLC9A3P2, 39 more genes
    nsv5980452copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,889,969-21,462,658 , GRCh38.p12 chr22: 18,339,130-21,108,369 LINC01637, BCRP7, 124 more genes
    nsv5969806insertion1nstd209human GRCh38 chr22: 20,927,192-20,927,192 , GRCh37.p13 chr22: 21,281,480-21,281,480 CRKL
    nsv5967784inversion1nstd209human GRCh38 chr22: 20,337,735-21,327,040 , GRCh37.p13 chr22: 20,325,258-21,681,329 , CRKL, 49 more genes
    nsv5961906copy number variation1nstd209human GRCh38 chr22: 20,952,084-20,952,248 , GRCh37.p13 chr22: 21,306,372-21,306,536 CRKL
    nsv5717683mobile element insertion1nstd211human GRCh38 chr22: 20,921,732-20,921,732 , GRCh37.p13 chr22: 21,276,020-21,276,020 CRKL
    nsv5716587mobile element insertion2nstd211human GRCh38 chr22: 20,934,831-20,934,831 , GRCh37.p13 chr22: 21,289,119-21,289,119 CRKL
    nsv5711004mobile element insertion1nstd211human GRCh38 chr22: 20,938,303-20,938,303 , GRCh37.p13 chr22: 21,292,591-21,292,591 CRKL
    nsv5673274copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,893,882-21,563,420 , GRCh38.p12 chr22: 18,339,130-21,209,131 UFD1-AS1, LOC100129254, 129 more genes
    nsv5673187copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr22: 18,900,688-21,351,637 , GRCh38.p12 chr22: 18,339,130-20,997,348 RN7SKP131, DGCR6, 114 more genes
    nsv5673185copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,893,882-21,571,027 , GRCh38.p12 chr22: 18,339,130-21,216,738 CCDC188, LOC107987325, 129 more genes
    nsv5671172insertion1nstd207human GRCh38 chr22: 20,934,830-20,934,830 , GRCh37.p13 chr22: 21,289,118-21,289,118 CRKL
    nsv5670785inversion1nstd207human GRCh38 chr22: 18,746,351-21,188,291 , GRCh37.p13 chr22: 18,733,864-21,542,580 , ARVCF, 114 more genes
    nsv5598631copy number variation1nstd207human GRCh38 chr22: 20,952,084-20,952,248 , GRCh37.p13 chr22: 21,306,372-21,306,536 CRKL
    nsv5546016copy number variation1nstd206human GRCh38 chr22: 20,689,282-21,312,400 , GRCh37.p13 chr22: 21,043,570-21,666,689 , BCRP2, 30 more genes
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