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Items: 1 to 20 of 318

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978189inversion1nstd209human GRCh38 chr21: 44,550,659-44,628,117 , GRCh37.p13 chr21: 45,970,542-46,048,034 , GRCh37.p13 chr21|NW_004775435.1: 53,982-131,440 TSPEAR, KRTAP10-4, 7 more genes
    nsv5977718insertion1nstd209human GRCh38 chr21: 44,592,514-44,592,514 , GRCh37.p13 chr21|NW_004775435.1: 95,837-95,837 , GRCh37.p13 chr21: 46,012,395-46,012,395 TSPEAR, KRTAP10-6
    nsv5970889inversion1nstd209human GRCh38 chr21: 44,591,798-44,601,087 , GRCh37.p13 chr21: 46,011,679-46,021,002 , GRCh37.p13 chr21|NW_004775435.1: 95,121-104,410 TSPEAR, KRTAP10-6, 1 more genes
    nsv5953827copy number variation1nstd209human GRCh38 chr21: 44,558,614-44,592,337 , GRCh37.p13 chr21|NW_004775435.1: 61,937-95,660 , GRCh37.p13 chr21: 45,978,497-46,012,218 TSPEAR, KRTAP10-4, 3 more genes
    nsv5871001copy number variation2nstd209human GRCh38 chr21: 44,589,050-44,590,149 , GRCh37.p13 chr21|NW_004775435.1: 92,373-93,472 , GRCh37.p13 chr21: 46,008,930-46,010,029 KRTAP10-6, TSPEAR
    nsv5671713insertion1nstd207human GRCh38 chr21: 44,591,838-44,591,838 , GRCh37.p13 chr21|NW_004775435.1: 95,161-95,161 , GRCh37.p13 chr21: 46,011,719-46,011,719 KRTAP10-6, TSPEAR
    nsv5670323insertion1nstd207human GRCh38 chr21: 44,591,870-44,591,870 , GRCh37.p13 chr21|NW_004775435.1: 95,193-95,193 , GRCh37.p13 chr21: 46,011,751-46,011,751 TSPEAR, KRTAP10-6
    nsv5559623inversion1nstd206human GRCh38 chr21: 44,549,786-44,628,795 , GRCh37.p13 chr21: 45,969,669-46,048,712 , GRCh37.p13 chr21|NW_004775435.1: 53,109-132,118 TSPEAR, KRTAP10-4, 7 more genes
    nsv5039150copy number variation1nstd200human GRCh38 chr21: 44,579,984-44,591,577 , GRCh37.p13 chr21|NW_004775435.1: 83,307-94,900 , GRCh37.p13 chr21: 45,999,861-46,011,458 KRTAP10-6, KRTAP10-5, 1 more genes
    nsv5039000copy number variation1nstd200human GRCh38 chr21: 44,497,091-44,687,158 , GRCh37.p13 chr21|NW_004775435.1: 414-190,479 , GRCh37.p13 chr21: 45,916,974-46,107,073 KRTAP12-1, KRTAP10-2, 18 more genes
    nsv5038397copy number variation1nstd200human GRCh38 chr21: 44,332,469-44,603,779 , GRCh37.p13 chr21: 45,752,352-45,916,560 TSPEAR-AS2, CFAP410, 17 more genes
    nsv4863454copy number variation1nstd200human GRCh37 chr21: 45,999,834-46,011,457 , GRCh38.p12 chr21: 44,579,957-44,591,576 KRTAP10-5, KRTAP10-6, 1 more genes
    nsv4762198insertion1nstd199human GRCh37 chr21: 46,011,972-46,011,972 , GRCh38.p12 chr21: 44,592,091-44,592,091 TSPEAR, KRTAP10-6
    nsv4749748copy number variation1nstd199human GRCh38.p12 chr21: 44,592,091-44,592,459 , GRCh37 chr21: 46,011,972-46,012,340 TSPEAR, KRTAP10-6
    nsv4730021copy number variation1nstd102humanPathogenic GRCh37 chr21: 14,629,063-48,090,317 , GRCh38.p12 chr21: 13,256,742-46,670,405 SLX9, LOC105372750, 619 more genes
    nsv4683666copy number variation1nstd102humanUncertain significance GRCh37 chr21: 45,725,202-46,131,429 , GRCh38.p12 chr21: 44,305,319-44,711,514 KRTAP10-8, KRTAP12-4, 30 more genes
    nsv4682565copy number variation1nstd102humanUncertain significance GRCh37 chr21: 45,725,202-46,234,019 , GRCh38.p12 chr21: 44,305,319-44,814,104 KRTAP10-2, TRPM2-AS, 33 more genes
    nsv4681891copy number variation1nstd102humanUncertain significance GRCh37 chr21: 43,792,871-46,330,697 , GRCh38.p12 chr21: 42,372,762-44,910,782 DNMT3L-AS1, WDR4, 100 more genes
    nsv4679058copy number variation1nstd189human GRCh37.p13 chr21: 14,468,835-48,129,895 , GRCh38.p12 chr21: 13,096,514-46,699,983 , ADARB1, 652 more genes
    nsv4676376copy number variation1nstd102humanPathogenic GRCh37 chr21: 43,472,147-48,097,372 , GRCh38.p12 chr21: 42,052,038-46,677,460 LOC101928369, MTND6P21, 157 more genes
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