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Items: 1 to 20 of 296

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112721copy number variation1nstd102humanPathogenic GRCh37 chrX: 47,179,068-54,424,785 , GRCh38.p12 chrX: 47,319,669-54,398,352 SNORA11E, SSX11P, 229 more genes
    nsv6112690copy number variation1nstd102humanPathogenic GRCh37 chrX: 60,000-155,234,966 , GRCh38.p12 chrX: 10,001-156,005,301 LOC105373176, ZFX-AS1, 2151 more genes
    nsv5882331copy number variation1nstd209human GRCh38 chrX: 49,640,631-49,701,976 , GRCh37.p13 chrX|NW_004070880.2: 1,830,060-1,891,405 , GRCh37.p13 chrX: 49,405,234-49,466,579 PAGE1, SALL1P1
    nsv5877274copy number variation1nstd209human GRCh38 chrX: 48,251,965-52,619,725 , GRCh37.p13 chrX|NW_004070877.1: 1-2,332,840 PLP2, SSXP8, 146 more genes
    nsv5869955copy number variation1nstd209human GRCh38 chrX: 49,689,782-49,690,012 , GRCh37.p13 chrX: 49,454,385-49,454,615 , GRCh37.p13 chrX|NW_004070880.2: 1,879,211-1,879,441 PAGE1
    nsv5669757copy number variation1nstd207human GRCh37.p13 chrX|NW_004070880.2: 1,879,373-1,879,540 , GRCh38 chrX: 49,689,944-49,690,111 , GRCh37.p13 chrX: 49,454,547-49,454,714 PAGE1
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 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
    nsv5415152copy number variation1nstd206human GRCh38 chrX: 49,689,028-49,690,029 , GRCh37.p13 chrX: 49,453,631-49,454,632 , GRCh37.p13 chrX|NW_004070880.2: 1,878,457-1,879,458 PAGE1
    nsv5381751copy number variation2nstd102humanUncertain significance GRCh37 chrX: 48,382,160-49,856,876 , GRCh38.p12 chrX: 48,523,772-50,092,219 EBP, MIR500A, 71 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
    nsv4728653copy number variation1nstd102humanPathogenic GRCh37 chrX: 48,102,202-52,685,635 , GRCh38.p12 chrX: 48,242,767-52,656,585 CCNB3, AKAP4, 150 more genes
    nsv4728488copy number variation1nstd102humanUncertain significance GRCh37 chrX: 49,293,398-49,636,361 , GRCh38.p12 chrX: 49,528,795-49,871,758 SALL1P1, GAGE12F, 11 more genes
    nsv4728486copy number variation1nstd102humanPathogenic GRCh37 chrX: 219,609-55,466,476 , GRCh38.p12 chrX: 302,942-55,440,043 CDK16, WASF4P, 772 more genes
    nsv4728251copy number variation1nstd102humanUncertain significance GRCh37 chrX: 49,360,237-49,636,361 , GRCh38.p12 chrX: 49,595,634-49,871,758 PAGE1, GAGE1, 4 more genes
    nsv4728228copy number variation1nstd102humanPathogenic GRCh37 chrX: 48,178,413-52,686,510 , GRCh38.p12 chrX: 48,318,978-52,657,460 MRPL32P1, LOC100421603, 142 more genes
    nsv4684016inversion1nstd191human GRCh37.p13 chrX: 32,933,886-87,244,324 , GRCh38 chrX: 32,915,769-87,989,324 , ABCB7, 816 more genes
    nsv4680157copy number variation1nstd189human GRCh37.p13 chrX: 48,059,259-52,748,576 , GRCh38.p12 chrX: 48,199,823-52,719,527 CACNA1F, CLCN5, 157 more genes
    nsv4674588copy number variation1nstd102humanPathogenic GRCh37 chrX: 539,722-55,509,385 , GRCh38.p12 chrX: 578,987-55,482,952 LOC392440, SSX4, 769 more genes
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