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Items: 1 to 20 of 307

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5938983copy number variation1nstd209human GRCh38 chr16: 70,703,365-70,703,417 , GRCh37.p13 chr16: 70,737,268-70,737,320 VAC14
    nsv5933236copy number variation1nstd209human GRCh38 chr16: 70,685,863-70,686,167 , GRCh37.p13 chr16: 70,719,766-70,720,070 MTSS2, VAC14
    nsv5710804mobile element insertion1nstd211human GRCh38 chr16: 70,708,480-70,708,480 , GRCh37.p13 chr16: 70,742,383-70,742,383 VAC14
    nsv5669930inversion1nstd207human GRCh38 chr16: 70,123,796-74,346,113 , GRCh37.p13 chr16: 70,157,699-74,380,011 , AARS1, 83 more genes
    nsv5557110sequence alteration1nstd206human GRCh38 chr16: 70,117,371-74,396,141 , GRCh37.p13 chr16: 70,151,274-74,430,039 , TAT, 84 more genes
    nsv5533252copy number variation1nstd206human GRCh38 chr16: 70,715,121-70,715,213 , GRCh37.p13 chr16: 70,749,024-70,749,116 VAC14
    nsv5523909copy number variation1nstd206human GRCh38 chr16: 70,727,847-70,727,932 , GRCh37.p13 chr16: 70,761,750-70,761,835 VAC14
    nsv5523457copy number variation1nstd206human GRCh38 chr16: 70,735,072-70,735,141 , GRCh37.p13 chr16: 70,768,975-70,769,044 VAC14
    nsv5517632copy number variation1nstd206human GRCh38 chr16: 70,704,184-70,704,425 , GRCh37.p13 chr16: 70,738,087-70,738,328 VAC14
    nsv5515145copy number variation1nstd206human GRCh38 chr16: 70,703,367-70,703,418 , GRCh37.p13 chr16: 70,737,270-70,737,321 VAC14
    nsv5427327mobile element insertion1nstd206human GRCh38 chr16: 70,708,480-70,708,531 , GRCh37.p13 chr16: 70,742,383-70,742,434 VAC14
    nsv5340072translocation1nstd200human GRCh37 chr16: 70,780,617-70,780,617 , GRCh37 chr16: 70,780,682-70,780,682 , GRCh38.p12 chr16: 70,746,779-70,746,779 , GRCh38.p12 chr16: 70,746,714-70,746,714 VAC14
    nsv5334379translocation1nstd200human GRCh37 chr16: 70,824,704-70,824,704 , GRCh37 chr16: 70,824,757-70,824,757 , GRCh38.p12 chr16: 70,790,854-70,790,854 , GRCh38.p12 chr16: 70,790,801-70,790,801 VAC14
    nsv5300588copy number variation1nstd204human GRCh37.p13 chr16: 70,802,537-70,805,125 , GRCh38.p13 chr16: 70,768,634-70,771,222 VAC14-AS1, VAC14
    nsv5284284copy number variation1nstd204human GRCh38.p13 chr16: 70,768,236-70,770,735 , GRCh37.p13 chr16: 70,802,139-70,804,638 VAC14-AS1, VAC14
    nsv5158076mobile element insertion1nstd203human GRCh38 chr16: 70,708,466-70,708,480 , GRCh37.p13 chr16: 70,742,369-70,742,383 VAC14
    nsv5156005mobile element insertion1nstd203human GRCh38 chr16: 70,767,286-70,767,305 , GRCh37.p13 chr16: 70,801,189-70,801,208 VAC14, VAC14-AS1
    nsv5148004mobile element insertion1nstd203human GRCh38 chr16: 70,741,446-70,741,461 , GRCh37.p13 chr16: 70,775,349-70,775,364 VAC14
    nsv5034683inversion1nstd200human GRCh38 chr16: 60,098,351-77,500,042 , GRCh37.p13 chr16: 60,132,255-77,533,939 , TRG-GCC2-5, 313 more genes
    nsv5032927inversion1nstd200human GRCh38 chr16: 70,715,776-70,715,962 , GRCh37.p13 chr16: 70,749,679-70,749,865 VAC14
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