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Items: 1 to 20 of 215

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5906616copy number variation1nstd209human GRCh38 chr4: 68,242,187-68,242,410 , GRCh37.p13 chr4: 69,107,905-69,108,128 TMPRSS11B
    nsv5893576copy number variation1nstd209human GRCh38 chr4: 67,920,462-75,134,545 , GRCh37.p13 chr4: 68,786,180-76,059,755 , DCK, 147 more genes
    nsv5675164mobile element insertion1nstd211human GRCh38 chr4: 68,243,620-68,243,620 , GRCh37.p13 chr4: 69,109,338-69,109,338 TMPRSS11B
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5614793insertion1nstd207human GRCh38 chr4: 68,242,306-68,242,306 , GRCh37.p13 chr4: 69,108,024-69,108,024 TMPRSS11B
    nsv5583958copy number variation1nstd207human GRCh38 chr4: 68,242,187-68,242,410 , GRCh37.p13 chr4: 69,107,905-69,108,128 TMPRSS11B
    nsv5463040copy number variation1nstd206human GRCh38 chr4: 68,242,203-68,242,411 , GRCh37.p13 chr4: 69,107,921-69,108,129 TMPRSS11B
    nsv5404864mobile element insertion1nstd206human GRCh38 chr4: 68,243,620-68,243,671 , GRCh37.p13 chr4: 69,109,338-69,109,389 TMPRSS11B
    nsv5346668translocation1nstd200human GRCh38 chr4: 68,242,411-68,242,411 , GRCh38 chr4: 68,242,203-68,242,203 , GRCh37.p13 chr4: 69,107,921-69,107,921 , GRCh37.p13 chr4: 69,108,129-69,108,129 TMPRSS11B
    nsv5341959translocation1nstd200human GRCh37 chr4: 69,107,921-69,107,921 , GRCh37 chr4: 69,108,129-69,108,129 , GRCh38.p12 chr4: 68,242,411-68,242,411 , GRCh38.p12 chr4: 68,242,203-68,242,203 TMPRSS11B
    nsv5320476translocation1nstd204human GRCh38.p13 chr4: 68,242,411-68,242,411 , GRCh38.p13 chr4: 68,242,203-68,242,203 , GRCh37.p13 chr4: 69,108,129-69,108,129 , GRCh37.p13 chr4: 69,107,921-69,107,921 TMPRSS11B
    nsv5098671mobile element insertion1nstd203human GRCh38 chr4: 68,243,606-68,243,620 , GRCh37.p13 chr4: 69,109,324-69,109,338 TMPRSS11B
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4922778copy number variation1nstd200human GRCh38 chr4: 68,046,584-68,288,946 , GRCh37.p13 chr4: 68,912,302-69,154,664 TMPRSS11B, TMPRSS11F, 6 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4800069copy number variation1nstd200human GRCh37 chr4: 68,912,302-69,154,664 , GRCh38.p12 chr4: 68,046,584-68,288,946 TMPRSS11B, TMPRSS11F, 6 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
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