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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3904985copy number variation1nstd102humanBenign GRCh37 chr22: 42,433,627-42,447,341 , GRCh38.p12 chr22: 42,037,623-42,051,337 WBP2NL
    nsv3909254copy number variation1nstd102humanBenign GRCh37 chr22: 42,435,868-42,447,341 , GRCh38.p12 chr22: 42,039,864-42,051,337 WBP2NL
    nsv3906905copy number variation1nstd102humanBenign GRCh37 chr22: 42,441,825-42,447,341 , GRCh38.p12 chr22: 42,045,821-42,051,337 WBP2NL
    nsv3892430copy number variation1nstd102humanBenign GRCh37 chr22: 42,441,890-42,447,341 , GRCh38.p12 chr22: 42,045,886-42,051,337 WBP2NL
    nsv3908301copy number variation1nstd102humanBenign GRCh37 chr22: 42,447,341-42,453,407 , GRCh38.p12 chr22: 42,051,337-42,057,403 WBP2NL, NAGA
    nsv3900214copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,151,555-51,195,728 , GRCh38.p12 chr22: 41,755,551-50,757,300 WBP2NL, TYMP, 218 more genes
    nsv6290298copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,321,321-51,244,066 , GRCh38.p12 chr22: 41,925,317-50,805,638 WBP2NL, CERK, 212 more genes
    nsv3912011copy number variation1nstd102humanPathogenic NCBI36 chr22: 40,597,093-49,525,130 , GRCh38 chr22: 41,871,143-50,739,836 , GRCh37 chr22: 42,267,147-51,178,264 WBP2NL, TUBGCP6, 213 more genes
    nsv5381149copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,333,802-51,195,728 , GRCh38.p12 chr22: 41,937,798-50,757,300 WBP2NL, RN7SKP80, 210 more genes
    nsv4351202copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,416,026-51,181,759 , GRCh38.p12 chr22: 42,020,022-50,743,331 WBP2NL, PLXNB2, 204 more genes
    nsv3893572copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,441,918-51,197,838 , GRCh38.p12 chr22: 42,045,914-50,759,410 WBP2NL, CYP2D8P, 206 more genes
    nsv5673276copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,440,000-43,780,000 , GRCh38.p12 chr22: 42,043,996-43,383,994 WBP2NL, RPL5P34, 48 more genes
    nsv5381088copy number variation1nstd102humanPathogenic GRCh37 chr22: 42,356,886-43,684,002 , GRCh38.p12 chr22: 41,960,882-43,287,996 WBP2NL, CYP2D8P, 49 more genes
    nsv3902776copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,054,667-51,243,435 , GRCh38.p12 chr22: 16,367,190-50,805,007 WBP2NL, LOC100419811, 1084 more genes
    nsv3894026copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,054,691-51,237,518 , GRCh38.p12 chr22: 16,367,190-50,799,090 WBP2NL, IGKV3OR22-2, 1084 more genes
    nsv3890411copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,054,691-51,237,463 , GRCh38.p12 chr22: 16,367,190-50,799,035 WBP2NL, RNU6-495P, 1084 more genes
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 WBP2NL, FBXO7, 1084 more genes
    nsv3902598copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,054,691-51,220,902 , GRCh38.p12 chr22: 16,367,190-50,782,474 WBP2NL, FABP5P11, 1084 more genes
    nsv3907231copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,114,244-51,211,392 , GRCh38.p12 chr22: 16,367,190-50,772,964 WBP2NL, DDTL, 1084 more genes
    nsv3890401copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,114,244-51,195,728 , GRCh38.p12 chr22: 16,367,190-50,757,300 WBP2NL, YPEL1, 1083 more genes
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