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Items: 1 to 20 of 482

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975321insertion1nstd209human GRCh38 chr17: 17,077,752-17,077,752 , GRCh37.p13 chr17: 16,981,066-16,981,066 MPRIP
    nsv5974534inversion1nstd209human GRCh38 chr17: 15,750,079-18,634,890 , GRCh37.p13 chr17: 15,653,393-18,538,203 , ADORA2B, 119 more genes
    nsv5935606copy number variation1nstd209human GRCh38 chr17: 17,114,780-17,114,867 , GRCh37.p13 chr17: 17,018,094-17,018,181 MPRIP
    nsv5933579copy number variation1nstd209human GRCh38 chr17: 16,936,959-20,558,118 , GRCh37.p13 chr17: 16,840,273-20,461,431 , FAM106B, 146 more genes
    nsv5714155mobile element insertion1nstd211human GRCh38 chr17: 17,186,053-17,186,053 , GRCh37.p13 chr17: 17,089,367-17,089,367 MPRIP
    nsv5695432mobile element insertion2nstd211human GRCh38 chr17: 17,077,770-17,077,770 , GRCh37.p13 chr17: 16,981,084-16,981,084 MPRIP
    nsv5665112inversion1nstd207human GRCh37.p13 chr17: 16,704,599-18,417,421 , GRCh38 chr17: 16,801,285-18,514,107 , DRG2, 71 more genes
    nsv5656848insertion1nstd207human GRCh38 chr17: 17,077,752-17,077,752 , GRCh37.p13 chr17: 16,981,066-16,981,066 MPRIP
    nsv5528094copy number variation1nstd206human GRCh38 chr17: 17,120,987-17,122,051 , GRCh37.p13 chr17: 17,024,301-17,025,365 MPRIP
    nsv5527396copy number variation1nstd206human GRCh38 chr17: 17,114,782-17,114,868 , GRCh37.p13 chr17: 17,018,096-17,018,182 MPRIP
    nsv5520199copy number variation1nstd206human GRCh38 chr17: 17,105,849-17,105,944 , GRCh37.p13 chr17: 17,009,163-17,009,258 MPRIP
    nsv5514365copy number variation1nstd206human GRCh38 chr17: 17,050,343-17,050,399 , GRCh37.p13 chr17: 16,953,657-16,953,713 MPRIP
    nsv5381800copy number variation1nstd102humanPathogenic GRCh37 chr17: 16,601,603-20,063,369 , GRCh38.p12 chr17: 16,698,289-20,160,056 COTL1P1, LOC105371551, 141 more genes
    nsv5358681translocation1nstd200human GRCh38 chr17: 17,116,937-17,116,937 , GRCh38 chr17: 17,119,243-17,119,243 , GRCh37.p13 chr17: 17,020,251-17,020,251 , GRCh37.p13 chr17: 17,022,557-17,022,557 MPRIP
    nsv5358680translocation1nstd200human GRCh38 chr17: 17,114,782-17,114,782 , GRCh38 chr17: 17,114,868-17,114,868 , GRCh37.p13 chr17: 17,018,182-17,018,182 , GRCh37.p13 chr17: 17,018,096-17,018,096 MPRIP
    nsv5358679translocation1nstd200human GRCh38 chr17: 17,105,849-17,105,849 , GRCh38 chr17: 17,105,944-17,105,944 , GRCh37.p13 chr17: 17,009,258-17,009,258 , GRCh37.p13 chr17: 17,009,163-17,009,163 MPRIP
    nsv5336578translocation1nstd200human GRCh37 chr17: 17,009,258-17,009,258 , GRCh37 chr17: 17,009,163-17,009,163 , GRCh38.p12 chr17: 17,105,944-17,105,944 , GRCh38.p12 chr17: 17,105,849-17,105,849 MPRIP
    nsv5313321copy number variation1nstd204human GRCh38.p13 chr17: 16,889,527-17,111,607 , GRCh37.p13 chr17: 16,792,841-17,014,921 TNFRSF13B, TBC1D27P, 3 more genes
    nsv5159037mobile element insertion1nstd203human GRCh38 chr17: 17,077,752-17,077,770 , GRCh37.p13 chr17: 16,981,066-16,981,084 MPRIP
    nsv5154739mobile element insertion1nstd203human GRCh38 chr17: 17,192,994-17,193,010 , GRCh37.p13 chr17: 17,096,308-17,096,324 MPRIP
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