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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
    nsv6116631copy number variation1nstd186human GRCh37 chrX: 53,478,192-53,491,595 , GRCh38.p12 chrX: 53,451,244-53,464,650 VTRNA3-1P, TIPINP1
    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
    nsv5885217copy number variation1nstd209human GRCh38 chrX: 53,451,220-53,464,670 , GRCh37.p13 chrX|NW_004070877.1: 3,164,335-3,177,785 , GRCh37.p13 chrX: 53,478,168-53,491,615 TIPINP1, VTRNA3-1P
    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
    nsv5416011copy number variation1nstd206human GRCh38 chrX: 53,451,200-53,464,708 , GRCh37.p13 chrX|NW_004070877.1: 3,164,315-3,177,823 , GRCh37.p13 chrX: 53,478,148-53,491,653 VTRNA3-1P, TIPINP1
    nsv5384554copy number variation1nstd186human GRCh37 chrX: 53,478,192-53,491,579 , GRCh38.p12 chrX: 53,451,244-53,464,634 VTRNA3-1P, TIPINP1
    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
    nsv4905515copy number variation1nstd200human GRCh38 chrX: 53,443,093-53,469,445 , GRCh37.p13 chrX: 53,470,040-53,496,392 , GRCh37.p13 chrX|NW_004070877.1: 3,156,208-3,182,560 VTRNA3-1P, TIPINP1
    nsv4782013copy number variation1nstd200human GRCh37 chrX: 53,470,040-53,496,392 , GRCh38.p12 chrX: 53,443,093-53,469,445 VTRNA3-1P, TIPINP1
    nsv4779755copy number variation1nstd200human GRCh37 chrX: 53,480,831-53,489,862 , GRCh38.p12 chrX: 53,453,884-53,462,921 VTRNA3-1P, TIPINP1
    nsv4779754copy number variation1nstd200human GRCh37 chrX: 53,478,192-53,491,579 , GRCh38.p12 chrX: 53,451,244-53,464,634 TIPINP1, VTRNA3-1P
    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
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