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Items: 1 to 20 of 223

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5958066insertion1nstd209human GRCh38 chr9: 96,456,781-96,456,781 , GRCh37.p13 chr9: 99,219,063-99,219,063 HABP4
    nsv5908650copy number variation1nstd209human GRCh38 chr9: 96,486,531-96,487,266 , GRCh37.p13 chr9: 99,248,813-99,249,548 HABP4
    nsv5698090mobile element insertion1nstd211human GRCh38 chr9: 96,456,781-96,456,781 , GRCh37.p13 chr9: 99,219,063-99,219,063 HABP4
    nsv5491786copy number variation1nstd206human GRCh38 chr9: 96,486,531-96,487,268 , GRCh37.p13 chr9: 99,248,813-99,249,550 HABP4
    nsv5491234copy number variation1nstd206human GRCh38 chr9: 96,484,847-96,484,908 , GRCh37.p13 chr9: 99,247,129-99,247,190 HABP4
    nsv5481988copy number variation1nstd206human GRCh38 chr9: 96,454,579-96,454,725 , GRCh37.p13 chr9: 99,216,861-99,217,007 HABP4
    nsv5381561copy number variation1nstd102humanPathogenic GRCh37 chr9: 97,834,573-107,199,088 , GRCh38.p12 chr9: 95,072,291-104,436,807 TBC1D2, ZNF782, 170 more genes
    nsv5372855translocation1nstd200human GRCh38 chr9: 96,450,225-96,450,225 , GRCh38 chr9: 96,450,118-96,450,118 , GRCh37.p13 chr9: 99,212,400-99,212,400 , GRCh37.p13 chr9: 99,212,507-99,212,507 HABP4
    nsv5317107copy number variation1nstd204human GRCh38.p13 chr9: 96,486,531-96,487,268 , GRCh37.p13 chr9: 99,248,813-99,249,550 HABP4
    nsv5254873copy number variation1nstd204human GRCh38.p13 chr9: 96,486,312-96,487,311 , GRCh37.p13 chr9: 99,248,594-99,249,593 HABP4
    nsv5241780copy number variation1nstd204human GRCh38.p13 chr9: 96,486,501-96,487,300 , GRCh37.p13 chr9: 99,248,783-99,249,582 HABP4
    nsv5194986mobile element insertion1nstd203human GRCh38 chr9: 96,472,089-96,472,099 , GRCh37.p13 chr9: 99,234,371-99,234,381 HABP4
    nsv5128352mobile element insertion1nstd203human GRCh38 chr9: 96,487,760-96,487,776 , GRCh37.p13 chr9: 99,250,042-99,250,058 HABP4
    nsv4982650copy number variation1nstd200human GRCh38 chr9: 96,486,531-96,487,268 , GRCh37.p13 chr9: 99,248,813-99,249,550 HABP4
    nsv4982649copy number variation1nstd200human GRCh38 chr9: 96,479,652-96,485,136 , GRCh37.p13 chr9: 99,241,934-99,247,418 HABP4
    nsv4982648copy number variation1nstd200human GRCh38 chr9: 96,453,286-96,457,917 , GRCh37.p13 chr9: 99,215,568-99,220,199 HABP4
    nsv4824140copy number variation1nstd200human GRCh37 chr9: 99,248,813-99,249,550 , GRCh38.p12 chr9: 96,486,531-96,487,268 HABP4
    nsv4824139copy number variation1nstd200human GRCh37 chr9: 99,244,093-99,244,399 , GRCh38.p12 chr9: 96,481,811-96,482,117 HABP4
    nsv4824138copy number variation1nstd200human GRCh37 chr9: 99,241,934-99,247,420 , GRCh38.p12 chr9: 96,479,652-96,485,138 HABP4
    nsv4824137copy number variation1nstd200human GRCh37 chr9: 99,215,568-99,220,199 , GRCh38.p12 chr9: 96,453,286-96,457,917 HABP4
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