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Items: 1 to 20 of 190

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967951inversion1nstd209human GRCh38 chr16: 13,469,401-22,726,308 , GRCh37.p13 chr16: 13,563,258-22,737,629 , ABCC6, 214 more genes
    nsv5929387copy number variation1nstd209human GRCh38 chr16: 20,698,055-24,692,430 , GRCh37.p13 chr16: 20,709,377-24,703,751 , ACSM1, 87 more genes
    nsv5654270insertion1nstd207human GRCh38 chr16: 20,831,800-20,831,800 , GRCh37.p13 chr16: 20,843,122-20,843,122 LOC105371121, REXO5
    nsv5529908copy number variation1nstd206human GRCh38 chr16: 20,847,054-20,850,615 , GRCh37.p13 chr16: 20,858,376-20,861,937 REXO5
    nsv5374385translocation1nstd200human GRCh38 chr16: 20,829,432-20,829,432 , GRCh38 chr13: 102,908,745-102,908,745 , GRCh37.p13 chr16: 20,840,754-20,840,754 , GRCh37.p13 chr13: 103,561,095-103,561,095 LOC105371121, REXO5
    nsv5343480translocation1nstd200human GRCh37 chr16: 20,840,754-20,840,754 , GRCh37 chr13: 103,561,090-103,561,090 , GRCh38.p12 chr16: 20,829,432-20,829,432 , GRCh38.p12 chr13: 102,908,740-102,908,740 LOC105371121, REXO5
    nsv5276359copy number variation1nstd204human GRCh38.p13 chr16: 20,820,467-20,821,998 , GRCh37.p13 chr16: 20,831,789-20,833,320 REXO5
    nsv5199516mobile element insertion1nstd203human GRCh38 chr16: 20,831,799-20,831,809 , GRCh37.p13 chr16: 20,843,121-20,843,131 LOC105371121, REXO5
    nsv5199354mobile element insertion1nstd203human GRCh38 chr16: 20,831,795-20,831,809 , GRCh37.p13 chr16: 20,843,117-20,843,131 LOC105371121, REXO5
    nsv5196840mobile element insertion1nstd203human GRCh38 chr16: 20,831,806-20,831,809 , GRCh37.p13 chr16: 20,843,128-20,843,131 REXO5, LOC105371121
    nsv5193862mobile element insertion1nstd203human GRCh38 chr16: 20,831,807-20,831,809 , GRCh37.p13 chr16: 20,843,129-20,843,131 LOC105371121, REXO5
    nsv5187903mobile element insertion1nstd203human GRCh38 chr16: 20,831,804-20,831,809 , GRCh37.p13 chr16: 20,843,126-20,843,131 LOC105371121, REXO5
    nsv5186954mobile element insertion1nstd203human GRCh38 chr16: 20,831,800-20,831,809 , GRCh37.p13 chr16: 20,843,122-20,843,131 REXO5, LOC105371121
    nsv5185986mobile element insertion1nstd203human GRCh38 chr16: 20,831,797-20,831,809 , GRCh37.p13 chr16: 20,843,119-20,843,131 LOC105371121, REXO5
    nsv5185685mobile element insertion1nstd203human GRCh38 chr16: 20,831,809-20,831,809 , GRCh37.p13 chr16: 20,843,131-20,843,131 LOC105371121, REXO5
    nsv5182849mobile element insertion1nstd203human GRCh38 chr16: 20,831,794-20,831,809 , GRCh37.p13 chr16: 20,843,116-20,843,131 REXO5, LOC105371121
    nsv5182638mobile element insertion1nstd203human GRCh38 chr16: 20,831,798-20,831,809 , GRCh37.p13 chr16: 20,843,120-20,843,131 LOC105371121, REXO5
    nsv5181902mobile element insertion1nstd203human GRCh38 chr16: 20,831,802-20,831,809 , GRCh37.p13 chr16: 20,843,124-20,843,131 LOC105371121, REXO5
    nsv5148631mobile element insertion1nstd203human GRCh38 chr16: 20,844,811-20,844,826 , GRCh37.p13 chr16: 20,856,133-20,856,148 REXO5
    nsv5003112copy number variation1nstd200human GRCh38 chr16: 20,768,058-20,856,205 , GRCh37.p13 chr16: 20,779,380-20,867,527 ACSM3, REXO5, 4 more genes
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