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Items: 1 to 20 of 275

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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
    nsv5422660copy number variation1nstd206human GRCh38 chrX: 52,729,096-52,920,707 , GRCh37.p13 chrX|NW_004070877.1: 2,442,211-2,633,822 , GRCh37.p13 chrX: 52,786,323-52,949,897 XAGE3, XAGE5, 7 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
    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
    nsv4730076inversion36nstd198human GRCh37.p13 chrX: 52,908,860-53,006,423 , GRCh38 chrX: 52,879,830-52,977,241 , GRCh37.p13 chrX|NW_004070877.1: 2,592,945-2,690,356 FAM156A, FAM156B
    nsv4728618copy number variation1nstd102humanUncertain significance GRCh37 chrX: 52,733,540-52,954,547 , GRCh38.p12 chrX: 52,704,490-52,925,359 LOC107985641, XAGE3, 9 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
    nsv4517807copy number variation1nstd166human GRCh37.p13 chrX: 52,816,998-53,003,000 , GRCh38.p12 chrX: 52,787,953-52,973,810 FAM156A, XAGE3, 5 more genes
    nsv4516767copy number variation1nstd166human GRCh37.p13 chrX: 52,836,999-52,929,000 , GRCh38.p12 chrX: 52,807,975-52,899,974 LOC107985641, EIF4A2P4, 3 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
    nsv4450580copy number variation1nstd102humanUncertain significance GRCh37 chrX: 51,476,578-53,087,050 , GRCh38.p12 chrX: 51,733,482-53,057,868 LOC100421603, LOC100420089, 45 more genes
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