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Items: 1 to 20 of 33

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095942copy number variation1nstd102humanPathogenic GRCh37 chr22: 37,480,315-37,485,842 , GRCh38.p12 chr22: 37,084,275-37,089,802 TMPRSS6
    nsv3892832copy number variation1nstd102humanBenign GRCh37 chr22: 37,492,201-37,500,643 , GRCh38.p12 chr22: 37,096,161-37,104,603 TMPRSS6
    nsv3905469copy number variation1nstd102humanBenign GRCh37 chr22: 37,493,729-37,499,692 , GRCh38.p12 chr22: 37,097,689-37,103,652 TMPRSS6
    nsv3896291copy number variation1nstd102humanBenign GRCh37 chr22: 37,492,201-37,494,205 , GRCh38.p12 chr22: 37,096,161-37,098,165 TMPRSS6
    nsv3901215copy number variation1nstd102humanBenign GRCh37 chr22: 37,493,675-37,494,205 , GRCh38.p12 chr22: 37,097,635-37,098,165 TMPRSS6
    nsv7148278copy number variation1nstd102humanPathogenic GRCh38 chr22: 37,098,319-37,127,846 , GRCh37.p13 chr22: 37,494,359-37,523,886 TMPRSS6, IL2RB
    nsv3892091copy number variation1nstd102humanBenign GRCh37 chr22: 37,494,420-37,534,734 , GRCh38.p12 chr22: 37,098,380-37,138,694 TMPRSS6, IL2RB
    nsv7095837copy number variation1nstd102humanUncertain significance GRCh37 chr22: 37,494,436-37,540,212 , GRCh38.p12 chr22: 37,098,396-37,144,172 TMPRSS6, IL2RB
    nsv3890312copy number variation1nstd102humanUncertain significance GRCh37 chr22: 37,485,062-37,618,530 , GRCh38.p12 chr22: 37,089,022-37,222,490 TMPRSS6, IL2RB, 3 more genes
    nsv3922128copy number variation1nstd102humanPathogenic GRCh37 chr22: 35,729,986-39,296,182 , NCBI36 chr22: 34,059,986-37,626,128 , GRCh38 chr22: 35,333,993-38,900,177 TMPRSS6, LOC102724378, 120 more genes
    nsv1398432copy number variation1nstd102humanPathogenic GRCh37 chr22: 35,680,095-38,098,981 , GRCh38.p12 chr22: 35,284,102-37,702,974 TMPRSS6, MTCO1P20, 74 more genes
    nsv7095836copy number variation3nstd102humanUncertain significance, Pathogenic GRCh37 chr22: 37,154,355-39,148,633 , GRCh38.p12 chr22: 36,758,311-38,752,628 TMPRSS6, CSF2RBP1, 80 more genes
    nsv3904443copy number variation1nstd102humanPathogenic GRCh37 chr22: 36,877,226-38,548,989 , GRCh38.p12 chr22: 36,481,179-38,152,982 TMPRSS6, LOC107985576, 63 more genes
    nsv3914747copy number variation1nstd102humanPathogenic NCBI36 chr22: 35,278,369-36,395,868 , GRCh38 chr22: 36,552,376-37,669,915 , GRCh37 chr22: 36,948,423-38,065,922 TMPRSS6, ELFN2, 35 more genes
    nsv3902776copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,054,667-51,243,435 , GRCh38.p12 chr22: 16,367,190-50,805,007 TMPRSS6, LOC100419811, 1084 more genes
    nsv3894026copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,054,691-51,237,518 , GRCh38.p12 chr22: 16,367,190-50,799,090 TMPRSS6, 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 TMPRSS6, 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 TMPRSS6, FBXO7, 1084 more genes
    nsv3902598copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,054,691-51,220,902 , GRCh38.p12 chr22: 16,367,190-50,782,474 TMPRSS6, FABP5P11, 1084 more genes
    nsv3907231copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,114,244-51,211,392 , GRCh38.p12 chr22: 16,367,190-50,772,964 TMPRSS6, DDTL, 1084 more genes
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