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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
    nsv5558396sequence alteration1nstd206human GRCh38 chrX: 56,236,832-56,736,431 , GRCh37.p13 chrX: 56,263,265-56,762,864 KLF8, UBQLN2, 3 more genes
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5376261translocation1nstd200human GRCh38 chrX: 56,561,988-56,561,988 , GRCh38 chrX: 56,564,916-56,564,916 , GRCh37.p13 chrX: 56,588,421-56,588,421 , GRCh37.p13 chrX: 56,591,349-56,591,349 UBQLN2
    nsv5376260translocation1nstd200human GRCh38 chrX: 56,561,572-56,561,572 , GRCh38 chrX: 56,565,053-56,565,053 , GRCh37.p13 chrX: 56,588,005-56,588,005 , GRCh37.p13 chrX: 56,591,486-56,591,486 UBQLN2
    nsv5059979copy number variation1nstd102humanPathogenic GRCh37 chrX: 56,469,080-155,233,731 , GRCh38.p12 chrX: 56,442,647-156,004,066 VDAC1P1, LOC105373299, 1364 more genes
    nsv5030775inversion1nstd200human GRCh38 chrX: 23,472,124-121,561,941 , GRCh37.p13 chrX: 23,490,241-120,695,795 , GPR173, 1350 more genes
    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
    nsv4674344copy number variation1nstd102humanUncertain significance GRCh37 chrX: 56,457,791-56,721,134 , GRCh38.p12 chrX: 56,431,358-56,694,701 UBQLN2
    nsv4578278inversion1nstd102humanLikely pathogenic GRCh37 chrX: 32,196,272-75,245,806 , GRCh38.p12 chrX: 32,178,155-76,025,971 ABCB7, ACTG1P10, 704 more genes
    nsv4576352mobile element insertion1nstd166human GRCh37.p13 chrX: 56,589,351-56,589,351 , GRCh38.p12 chrX: 56,562,918-56,562,918 UBQLN2
    nsv4452472copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-61,877,279 , GRCh38.p12 chrX: 251,879-62,657,809 MIR660, RNU6-1321P, 802 more genes
    nsv4451374copy number variation1nstd102humanUncertain significance GRCh37 chrX: 56,457,791-57,976,114 , GRCh38.p12 chrX: 56,431,358-57,949,680 UQCRBP1, SPIN2A, 14 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
    nsv4367211copy number variation1nstd173human GRCh37 chrX: 168,547-155,233,756 , GRCh38.p12 chrX: 251,880-156,004,091 , MIR421, 2192 more genes
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