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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5545340insertion1nstd206human GRCh38 chrX: 55,743,945-55,743,962 , GRCh37.p13 chrX: 55,770,378-55,770,395 RRAGB
    nsv5426636copy number variation1nstd206human GRCh38 chrX: 55,728,461-55,728,528 , GRCh37.p13 chrX: 55,754,894-55,754,961 RRAGB
    nsv5420731copy number variation1nstd206human GRCh38 chrX: 55,735,041-55,735,275 , GRCh37.p13 chrX: 55,761,474-55,761,708 RRAGB
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5059968copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-56,457,794 , GRCh38.p12 chrX: 251,879-56,431,361 PAGE3, METTL15P3, 785 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    nsv4787571copy number variation1nstd200human GRCh37 chrX: 55,761,474-55,761,708 , GRCh38.p12 chrX: 55,735,041-55,735,275 RRAGB
    nsv4787570copy number variation1nstd200human GRCh37 chrX: 55,741,900-55,743,156 , GRCh38.p12 chrX: 55,715,467-55,716,723 RRAGB
    nsv4728499copy number variation1nstd102humanPathogenic GRCh37 chrX: 55,507,789-155,198,481 , GRCh38.p12 chrX: 55,481,356-155,968,816 GABRE, RN7SL325P, 1371 more genes
    nsv4684016inversion1nstd191human GRCh37.p13 chrX: 32,933,886-87,244,324 , GRCh38 chrX: 32,915,769-87,989,324 , ABCB7, 816 more genes
    nsv4578278inversion1nstd102humanLikely pathogenic GRCh37 chrX: 32,196,272-75,245,806 , GRCh38.p12 chrX: 32,178,155-76,025,971 ABCB7, ACTG1P10, 704 more genes
    nsv4565798mobile element insertion1nstd166human GRCh37.p13 chrX: 55,777,259-55,777,259 , GRCh38.p12 chrX: 55,750,826-55,750,826 RRAGB
    nsv4534897insertion1nstd166human GRCh37.p13 chrX: 55,754,894-55,754,894 , GRCh38.p12 chrX: 55,728,461-55,728,461 RRAGB
    nsv4452472copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-61,877,279 , GRCh38.p12 chrX: 251,879-62,657,809 MIR660, RNU6-1321P, 802 more genes
    nsv4450820copy number variation1nstd102humanPathogenic GRCh37 chrX: 40,572,613-92,796,528 , GRCh38.p12 chrX: 40,713,361-93,541,529 HNRNPA1P25, MPV17L2P1, 755 more genes
    nsv4450523copy number variation1nstd102humanUncertain significance GRCh37 chrX: 54,941,868-155,233,731 , GRCh38.p12 chrX: 54,915,435-156,004,066 LOC105373348, MIR548AN, 1396 more genes
    nsv4380296copy number variation3nstd173human GRCh37 chrX: 168,547-155,233,756 , GRCh38.p12 chrX: 251,880-156,004,091 , RPL31P63, 2192 more genes
    nsv4375765copy number variation1nstd173human GRCh37 chrX: 54,867,393-62,897,297 , GRCh38.p12 chrX: 54,840,960-63,677,417 , SPIN3, 61 more genes
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