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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4455609copy number variation1nstd102humanPathogenic GRCh37 chr6: 123,551,934-123,597,121 , GRCh38.p12 chr6: 123,230,789-123,275,976 TRDN
    nsv3875594copy number variation1nstd102humanBenign GRCh37 chr6: 123,560,579-123,592,852 , GRCh38.p12 chr6: 123,239,434-123,271,707 TRDN
    nsv3871177copy number variation1nstd102humanBenign GRCh37 chr6: 123,592,333-123,593,097 , GRCh38.p12 chr6: 123,271,188-123,271,952 TRDN
    nsv3882027copy number variation1nstd102humanBenign GRCh37 chr6: 123,592,333-123,593,044 , GRCh38.p12 chr6: 123,271,188-123,271,899 TRDN
    nsv6312225copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,573,537-123,595,835 , GRCh38.p12 chr6: 123,252,392-123,274,690 TRDN
    nsv7097178copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,818,318-123,825,066 , GRCh38.p12 chr6: 123,497,173-123,503,921 TRDN
    nsv5381381copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,818,328-123,825,056 , GRCh38.p12 chr6: 123,497,183-123,503,911 TRDN
    nsv4681322copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,539,736-123,545,286 , GRCh38.p12 chr6: 123,218,591-123,224,141 TRDN
    nsv7097037copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,833,428-123,837,371 , GRCh38.p12 chr6: 123,512,283-123,516,226 TRDN
    nsv6312023copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,581,598-123,581,802 , GRCh38.p12 chr6: 123,260,453-123,260,657 TRDN
    nsv7097312copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,687,260-123,687,347 , GRCh38.p12 chr6: 123,366,115-123,366,202 TRDN
    nsv7097313copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,703,243-123,703,312 , GRCh38.p12 chr6: 123,382,098-123,382,167 TRDN
    nsv7097177copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,581,737-123,581,803 , GRCh38.p12 chr6: 123,260,592-123,260,658 TRDN
    nsv7097568copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,573,537-123,573,600 , GRCh38.p12 chr6: 123,252,392-123,252,455 TRDN
    nsv4683798copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,818,328-123,833,517 , GRCh38.p12 chr6: 123,497,183-123,512,372 TRDN
    nsv7097569copy number variation1nstd102humanUncertain significance GRCh37 chr6: 123,580,749-123,595,835 , GRCh38.p12 chr6: 123,259,604-123,274,690 TRDN
    nsv3874032copy number variation1nstd102humanUncertain significance GRCh38 chr6: 123,265,298-123,267,771 , GRCh37 chr6: 123,586,443-123,588,916 TRDN
    nsv6634722delins1nstd102humanUncertain significance GRCh38 chr6: 123,512,258-123,512,312 , GRCh37 chr6: 123,833,403-123,833,457 TRDN
    nsv3889128copy number variation1nstd102humanBenign GRCh37 chr6: 123,556,891-123,753,606 , GRCh38.p12 chr6: 123,235,746-123,432,461 TRDN, LOC105377984
    nsv3872480copy number variation1nstd102humanBenign GRCh37 chr6: 123,560,579-123,669,127 , GRCh38.p12 chr6: 123,239,434-123,347,982 TRDN, LOC105377984
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