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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5929694copy number variation1nstd209human GRCh38 chr16: 88,697,477-88,697,549 , GRCh37.p13 chr16: 88,763,885-88,763,957 RNF166
    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
    nsv5533319copy number variation1nstd206human GRCh38 chr16: 88,697,481-88,697,550 , GRCh37.p13 chr16: 88,763,889-88,763,958 RNF166
    nsv5518742copy number variation1nstd206human GRCh38 chr16: 88,701,111-88,701,178 , GRCh37.p13 chr16: 88,767,519-88,767,586 RNF166
    nsv5358506translocation1nstd200human GRCh38 chr16: 88,701,178-88,701,178 , GRCh38 chr16: 88,701,111-88,701,111 , GRCh37.p13 chr16: 88,767,519-88,767,519 , GRCh37.p13 chr16: 88,767,586-88,767,586 RNF166
    nsv5358505translocation1nstd200human GRCh38 chr16: 88,697,481-88,697,481 , GRCh38 chr16: 88,697,550-88,697,550 , GRCh37.p13 chr16: 88,763,889-88,763,889 , GRCh37.p13 chr16: 88,763,958-88,763,958 RNF166
    nsv5333369translocation1nstd200human GRCh37 chr16: 88,763,958-88,763,958 , GRCh37 chr16: 88,763,889-88,763,889 , GRCh38.p12 chr16: 88,697,481-88,697,481 , GRCh38.p12 chr16: 88,697,550-88,697,550 RNF166
    nsv5325537translocation1nstd204human GRCh38.p13 chr16: 88,697,550-88,697,550 , GRCh38.p13 chr16: 88,697,481-88,697,481 , GRCh37.p13 chr16: 88,763,958-88,763,958 , GRCh37.p13 chr16: 88,763,889-88,763,889 RNF166
    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
    nsv4851013copy number variation1nstd200human GRCh37 chr16: 88,767,519-88,767,586 , GRCh38.p12 chr16: 88,701,111-88,701,178 RNF166
    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
    nsv4631762copy number variation1nstd183human GRCh37 chr16: 88,760,632-88,773,514 , GRCh38.p12 chr16: 88,694,224-88,707,106 CTU2, RNF166
    nsv4630604copy number variation1nstd183human GRCh37 chr16: 88,770,621-88,909,788 , GRCh38.p12 chr16: 88,704,213-88,843,380 , MIR4722, 9 more genes
    nsv4626010copy number variation2nstd183human GRCh37 chr16: 88,705,417-88,830,206 , GRCh38.p12 chr16: 88,639,009-88,763,798 PIEZO1, MIR4722, 9 more genes
    nsv4622587copy number variation1nstd183human GRCh37 chr16: 88,772,905-88,772,992 , GRCh38.p12 chr16: 88,706,497-88,706,584 CTU2, RNF166
    nsv4619776copy number variation1nstd183human GRCh37 chr16: 88,772,789-88,772,992 , GRCh38.p12 chr16: 88,706,381-88,706,584 RNF166, CTU2
    nsv4456065copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,453,448-89,569,215 , GRCh38.p12 chr16: 88,387,040-89,502,807 LOC101927863, LINC00304, 45 more genes
    nsv4455948copy number variation1nstd102humanUncertain significance GRCh37 chr16: 87,848,902-88,809,407 , GRCh38.p12 chr16: 87,815,296-88,742,999 CYBA, BANP, 27 more genes
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