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Items: 1 to 20 of 271

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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
    nsv5882057copy number variation1nstd209human GRCh38 chrX: 52,862,950-55,652,570 , GRCh37.p13 chrX: 52,891,979-54,424,077 , GRCh37.p13 chrX|NW_004070877.1: 2,576,065-4,110,759 , MIRLET7F2, 64 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
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5381720copy number variation1nstd102humanUncertain significance GRCh37 chrX: 53,560,270-53,622,363 , GRCh38.p12 chrX: 53,533,309-53,595,403 MIRLET7F2, HUWE1, 1 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
    nsv4769309copy number variation1nstd102humanPathogenic GRCh37 chrX: 52,923,471-53,765,589 , GRCh38.p12 chrX: 52,894,442-53,738,647 TSPYL2, SMC1A, 20 more genes
    nsv4728719copy number variation1nstd102humanPathogenic GRCh37 chrX: 53,188,785-54,049,698 , GRCh38.p12 chrX: 53,159,603-54,023,265 MIR6857, MIR6895, 16 more genes
    nsv4728662copy number variation1nstd102humanPathogenic GRCh37 chrX: 53,188,785-53,934,760 , GRCh38.p12 chrX: 53,159,603-53,908,342 KDM5C, MIR6857, 15 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
    nsv4684016inversion1nstd191human GRCh37.p13 chrX: 32,933,886-87,244,324 , GRCh38 chrX: 32,915,769-87,989,324 , ABCB7, 816 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
    nsv4578278inversion1nstd102humanLikely pathogenic GRCh37 chrX: 32,196,272-75,245,806 , GRCh38.p12 chrX: 32,178,155-76,025,971 ABCB7, ACTG1P10, 704 more genes
    nsv4517841copy number variation1nstd166human GRCh37.p13 chrX: 53,552,999-53,623,500 , GRCh38.p12 chrX: 53,526,034-53,596,540 HUWE1, MIR98, 1 more genes
    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
    nsv4449960copy number variation1nstd102humanPathogenic GRCh37 chrX: 53,384,424-54,103,704 , GRCh38.p12 chrX: 53,357,501-54,077,271 MIR6857, FAM120C, 11 more genes
    nsv4384325copy number variation1nstd173human GRCh37 chrX: 53,556,883-53,627,781 , GRCh38.p12 chrX: 53,529,918-53,600,821 MIR98, HUWE1, 1 more genes
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