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Items: 1 to 20 of 487

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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
    nsv5957379insertion1nstd209human GRCh38 chrX: 46,923,393-46,923,393 , GRCh37.p13 chrX: 46,782,828-46,782,828 , GRCh37.p13 chrX|NW_004166866.1: 172,954-172,954 JADE3
    nsv5885048copy number variation1nstd209human GRCh38 chrX: 46,999,397-46,999,472 , GRCh37.p13 chrX|NW_004166866.1: 248,958-249,033 , GRCh37.p13 chrX: 46,858,799-46,858,874 JADE3
    nsv5882824copy number variation1nstd209human GRCh38 chrX: 44,722,720-48,672,672 , GRCh37.p13 chrX: 44,581,966-47,619,970 ZNF674-AS1, CDK16, 115 more genes
    nsv5874995copy number variation1nstd209human GRCh38 chrX: 46,935,144-46,936,228 , GRCh37.p13 chrX: 46,794,579-46,795,663 , GRCh37.p13 chrX|NW_004166866.1: 184,705-185,789 JADE3
    nsv5873682copy number variation1nstd209human GRCh38 chrX: 41,560,623-47,265,899 , GRCh37.p13 chrX: 41,419,876-47,125,298 , CTNNBL1P1, 80 more genes
    nsv5717670mobile element insertion2nstd211human GRCh38 chrX: 47,045,672-47,045,672 , GRCh37.p13 chrX: 46,905,074-46,905,074 , GRCh37.p13 chrX|NW_004166866.1: 295,233-295,233 JADE3
    nsv5667627copy number variation1nstd207human GRCh37.p13 chrX|NW_004166866.1: 184,705-185,789 , GRCh38 chrX: 46,935,144-46,936,228 , GRCh37.p13 chrX: 46,794,579-46,795,663 JADE3
    nsv5616522insertion1nstd207human GRCh38 chrX: 46,999,436-46,999,436 , GRCh37.p13 chrX|NW_004166866.1: 248,997-248,997 , GRCh37.p13 chrX: 46,858,838-46,858,838 JADE3
    nsv5562478sequence alteration1nstd206human GRCh38 chrX: 45,310,830-84,506,186 , GRCh37.p13 chrX: 45,170,075-83,761,194 , AR, 649 more genes
    nsv5556729sequence alteration1nstd206human GRCh37.p13 chrX|NW_004166866.1: 111,970-469,972 , GRCh38 chrX: 46,862,409-47,356,182 , GRCh37.p13 chrX: 46,721,844-47,079,810 USP11, RGN, 16 more genes
    nsv5553321insertion1nstd206human GRCh38 chrX: 47,011,831-47,011,831 , GRCh37.p13 chrX: 46,871,233-46,871,233 , GRCh37.p13 chrX|NW_004166866.1: 261,392-261,392 JADE3
    nsv5430717copy number variation1nstd206human GRCh38 chrX: 46,994,095-46,994,474 , GRCh37.p13 chrX|NW_004166866.1: 243,656-244,035 , GRCh37.p13 chrX: 46,853,497-46,853,876 JADE3
    nsv5429858copy number variation1nstd206human GRCh38 chrX: 46,935,117-46,936,257 , GRCh37.p13 chrX|NW_004166866.1: 184,678-185,818 , GRCh37.p13 chrX: 46,794,552-46,795,692 JADE3
    nsv5425906copy number variation1nstd206human GRCh38 chrX: 47,024,013-47,024,108 , GRCh37.p13 chrX: 46,883,415-46,883,510 , GRCh37.p13 chrX|NW_004166866.1: 273,574-273,669 JADE3
    nsv5424363copy number variation1nstd206human GRCh38 chrX: 46,913,070-46,913,253 , GRCh37.p13 chrX|NW_004166866.1: 162,631-162,814 , GRCh37.p13 chrX: 46,772,505-46,772,688 JADE3
    nsv5416491copy number variation1nstd206human GRCh38 chrX: 39,941,083-72,578,519 , GRCh37.p13 chrX: 39,800,337-71,530,833 , USP51, 564 more genes
    nsv5415191copy number variation1nstd206human GRCh38 chrX: 46,998,858-47,000,942 , GRCh37.p13 chrX|NW_004166866.1: 248,419-250,503 , GRCh37.p13 chrX: 46,858,260-46,860,344 JADE3
    nsv5382540copy number variation1nstd186human GRCh37 chrX: 46,794,602-46,795,603 , GRCh38.p12 chrX: 46,935,167-46,936,168 JADE3
    nsv5381699copy number variation1nstd102humanUncertain significance GRCh37 chrX: 46,696,536-47,436,910 , GRCh38.p12 chrX: 46,837,101-47,577,511 LINC01560, LOC105373194, 25 more genes
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