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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6116656mobile element insertion1nstd186human GRCh37 chr16: 70,497,853-70,497,853 , GRCh38.p12 chr16: 70,463,950-70,463,950 FCSK
    nsv5942837copy number variation1nstd209human GRCh38 chr16: 70,455,784-70,456,911 , GRCh37.p13 chr16: 70,489,687-70,490,814 FCSK
    nsv5940084copy number variation1nstd209human GRCh38 chr16: 70,460,625-70,462,545 , GRCh37.p13 chr16: 70,494,528-70,496,448 FCSK
    nsv5936357copy number variation1nstd209human GRCh38 chr16: 70,453,320-70,453,451 , GRCh37.p13 chr16: 70,487,223-70,487,354 FCSK
    nsv5882858copy number variation1nstd209human GRCh38 chr16: 70,460,588-70,462,387 , GRCh37.p13 chr16: 70,494,491-70,496,290 FCSK
    nsv5877601copy number variation1nstd209human GRCh38 chr16: 70,455,911-70,456,910 , GRCh37.p13 chr16: 70,489,814-70,490,813 FCSK
    nsv5712905mobile element insertion2nstd211human GRCh38 chr16: 70,463,965-70,463,965 , GRCh37.p13 chr16: 70,497,868-70,497,868 FCSK
    nsv5704695mobile element insertion1nstd211human GRCh38 chr16: 70,461,094-70,461,094 , GRCh37.p13 chr16: 70,494,997-70,494,997 FCSK
    nsv5669930inversion1nstd207human GRCh38 chr16: 70,123,796-74,346,113 , GRCh37.p13 chr16: 70,157,699-74,380,011 , AARS1, 83 more genes
    nsv5653941insertion1nstd207human GRCh38 chr16: 70,453,320-70,453,320 , GRCh37.p13 chr16: 70,487,223-70,487,223 FCSK
    nsv5557110sequence alteration1nstd206human GRCh38 chr16: 70,117,371-74,396,141 , GRCh37.p13 chr16: 70,151,274-74,430,039 , TAT, 84 more genes
    nsv5555930sequence alteration1nstd206human GRCh38 chr16: 70,461,094-70,461,094 , GRCh37.p13 chr16: 70,494,997-70,494,997 FCSK
    nsv5535010insertion1nstd206human GRCh38 chr16: 70,461,090-70,461,090 , GRCh37.p13 chr16: 70,494,993-70,494,993 FCSK
    nsv5527119copy number variation1nstd206human GRCh38 chr16: 70,455,805-70,456,881 , GRCh37.p13 chr16: 70,489,708-70,490,784 FCSK
    nsv5514352copy number variation1nstd206human GRCh38 chr16: 70,453,301-70,453,458 , GRCh37.p13 chr16: 70,487,204-70,487,361 FCSK
    nsv5425592mobile element insertion1nstd206human GRCh38 chr16: 70,463,950-70,463,950 , GRCh37.p13 chr16: 70,497,853-70,497,853 FCSK
    nsv5390848copy number variation3nstd186human GRCh37 chr16: 70,487,204-70,487,361 , GRCh38.p12 chr16: 70,453,301-70,453,458 FCSK
    nsv5211349mobile element deletion1nstd204human GRCh38.p13 chr16: 70,465,368-70,465,691 , GRCh37.p13 chr16: 70,499,271-70,499,594 FCSK
    nsv5159960mobile element insertion1nstd203human GRCh38 chr16: 70,463,965-70,463,965 , GRCh37.p13 chr16: 70,497,868-70,497,868 FCSK
    nsv5157645mobile element insertion1nstd203human GRCh38 chr16: 70,463,949-70,463,965 , GRCh37.p13 chr16: 70,497,852-70,497,868 FCSK
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