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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5381762copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,284,464-141,018,984 , GRCh38.p12 chr9: 136,390,012-138,124,532 ARRDC1, SETP5, 101 more genes
    nsv5343779translocation1nstd200human GRCh37 chr9: 139,739,122-139,739,122 , GRCh37 chr9: 139,742,106-139,742,106 , GRCh38.p12 chr9: 136,847,654-136,847,654 , GRCh38.p12 chr9: 136,844,670-136,844,670 AJM1, PHPT1
    nsv5320726translocation1nstd204human GRCh37.p13 chr9: 139,739,122-139,739,122 , GRCh37.p13 chr9: 139,742,105-139,742,105 , GRCh38.p13 chr9: 136,844,670-136,844,670 , GRCh38.p13 chr9: 136,847,653-136,847,653 PHPT1, AJM1
    nsv5315985copy number variation1nstd204human GRCh37.p13 chr9: 139,739,315-139,742,174 , GRCh38.p13 chr9: 136,844,863-136,847,722 PHPT1, AJM1
    nsv5260219copy number variation1nstd204human GRCh38.p13 chr9: 136,844,642-136,847,496 , GRCh37.p13 chr9: 139,739,094-139,741,948 PHPT1, AJM1
    nsv5243680copy number variation1nstd204human GRCh38.p13 chr9: 136,802,801-136,886,500 , GRCh37.p13 chr9: 139,697,253-139,780,952 CCDC183, AJM1, 11 more genes
    nsv5243007copy number variation1nstd204human GRCh38.p13 chr9: 136,845,001-137,273,000 , GRCh37.p13 chr9: 139,739,453-140,167,452 ENTPD2, LINC02908, 43 more genes
    nsv4985870copy number variation1nstd200human GRCh38 chr9: 136,632,294-136,850,190 , GRCh37.p13 chr9: 139,526,746-139,744,642 CCDC183, PHPT1, 25 more genes
    nsv4985869copy number variation1nstd200human GRCh38 chr9: 136,591,087-136,947,348 , GRCh37.p13 chr9: 139,485,539-139,841,800 LOC102724193, AJM1, 34 more genes
    nsv4840157copy number variation1nstd200human GRCh37 chr9: 139,739,325-139,742,169 , GRCh38.p12 chr9: 136,844,873-136,847,717 AJM1, PHPT1
    nsv4768352copy number variation1nstd102humanPathogenic GRCh37 chr9: 139,018,777-141,018,984 , GRCh38.p12 chr9: 136,126,931-138,124,532 MIR6722, EXD3, 108 more genes
    nsv4729067copy number variation1nstd102humanUncertain significance GRCh37 chr9: 139,420,166-139,787,562 , GRCh38.p12 chr9: 136,525,714-136,893,110 LCN6, LCN15, 34 more genes
    nsv4685995copy number variation1nstd102humanPathogenic GRCh37 chr9: 138,225,001-141,015,001 , GRCh38.p12 chr9: 135,333,155-138,120,549 TPRN, CCDC183, 137 more genes
    nsv4683252copy number variation2nstd102humanUncertain significance GRCh37 chr9: 138,594,085-140,062,314 , GRCh38.p12 chr9: 135,702,239-137,167,862 SAPCD2, MIR3621, 81 more genes
    nsv4681206copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chr9: 138,645,763-140,729,425 , GRCh38.p12 chr9: 135,753,917-137,834,973 DPP7, MIR4673, 112 more genes
    nsv4637189copy number variation1nstd186human GRCh37 chr9: 139,738,787-139,748,879 , GRCh38.p12 chr9: 136,844,335-136,854,427 PHPT1, MAMDC4, 1 more genes
    nsv4617821copy number variation1nstd183human GRCh37 chr9: 139,734,760-139,744,534 , GRCh38.p12 chr9: 136,840,308-136,850,082 AJM1, RABL6, 1 more genes
    nsv4607054copy number variation1nstd183human GRCh37 chr9: 139,743,160-139,745,030 , GRCh38.p12 chr9: 136,848,708-136,850,578 MAMDC4, PHPT1
    nsv4598790copy number variation1nstd183human GRCh37 chr9: 139,744,985-139,747,909 , GRCh38.p12 chr9: 136,850,533-136,853,457 MAMDC4, PHPT1
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
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