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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6126598copy number variation1nstd186human GRCh37 chr16: 88,870,038-88,870,090 , GRCh38.p12 chr16: 88,803,630-88,803,682 CDT1
    nsv5928415copy number variation1nstd209human GRCh38 chr16: 88,793,529-88,831,958 , GRCh37.p13 chr16: 88,859,937-88,898,366 , APRT, 2 more genes
    nsv5879270copy number variation1nstd209human GRCh38 chr16: 88,802,995-88,811,297 , GRCh37.p13 chr16: 88,869,403-88,877,705 CDT1, APRT
    nsv5871668copy number variation1nstd209human GRCh38 chr16: 88,797,195-88,802,594 , GRCh37.p13 chr16: 88,863,603-88,869,002 CDT1
    nsv5673007copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,709,737-89,220,635 , GRCh38.p12 chr16: 88,643,329-89,154,227 MIR4722, PIEZO1, 23 more genes
    nsv5522014copy number variation1nstd206human GRCh38 chr16: 88,803,630-88,803,682 , GRCh37.p13 chr16: 88,870,038-88,870,090 CDT1
    nsv5516784copy number variation1nstd206human GRCh38 chr16: 88,746,102-88,896,171 , GRCh37.p13 chr16: 88,812,510-88,962,579 , 10 more genes
    nsv5308413copy number variation1nstd204human GRCh38.p13 chr16: 88,790,167-88,812,229 , GRCh37.p13 chr16: 88,856,575-88,878,637 , CDT1, 2 more genes
    nsv5296537copy number variation1nstd204human GRCh38.p13 chr16: 88,796,995-88,811,604 , GRCh37.p13 chr16: 88,863,403-88,878,012 CDT1, APRT
    nsv5289947copy number variation1nstd204human GRCh38.p13 chr16: 88,668,401-89,192,400 , GRCh37.p13 chr16: 88,734,809-89,258,808 , RNF166, 26 more genes
    nsv5287779copy number variation1nstd204human GRCh38.p13 chr16: 88,301,301-89,068,700 , GRCh37.p13 chr16: 88,334,907-89,135,108 , ZFPM1-AS1, 33 more genes
    nsv5286032copy number variation1nstd204human GRCh38.p13 chr16: 88,791,401-89,007,000 , GRCh37.p13 chr16: 88,857,809-89,073,408 , APRT, 12 more genes
    nsv5015062copy number variation1nstd200human GRCh38 chr16: 88,802,150-88,803,356 , GRCh37.p13 chr16: 88,868,558-88,869,764 CDT1
    nsv5015051copy number variation1nstd200human GRCh38 chr16: 88,770,796-88,862,257 , GRCh37.p13 chr16: 88,837,204-88,928,665 , APRT, 7 more genes
    nsv5013564copy number variation1nstd200human GRCh38 chr16: 88,793,529-88,831,963 , GRCh37.p13 chr16: 88,859,937-88,898,371 , CDT1, 2 more genes
    nsv5013563copy number variation1nstd200human GRCh38 chr16: 88,746,102-88,896,171 , GRCh37.p13 chr16: 88,812,510-88,962,579 , CBFA2T3, 10 more genes
    nsv4864376copy number variation1nstd200human GRCh37 chr16: 88,812,510-88,962,579 , GRCh38.p12 chr16: 88,746,102-88,896,171 , CDT1, 10 more genes
    nsv4851020copy number variation1nstd200human GRCh37 chr16: 88,868,558-88,869,764 , GRCh38.p12 chr16: 88,802,150-88,803,356 CDT1
    nsv4729945copy number variation1nstd102humanUncertain significance GRCh37 chr16: 88,222,732-90,155,062 , GRCh38.p12 chr16: 88,189,126-90,088,654 SNORD68, LOC105371412, 75 more genes
    nsv4685754copy number variation1nstd102humannot provided GRCh37 chr16: 61,524,229-90,155,062 , GRCh38.p12 chr16: 61,490,325-90,088,654 LOC100422319, MLYCD, 547 more genes
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