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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112700copy number variation1nstd102humanPathogenic GRCh38 chr16: 46,385,317-61,223,349 , GRCh37.p13 chr16: 46,419,229-61,257,253 CPNE2, USB1, 275 more genes
    nsv5201477mobile element deletion1nstd204human GRCh38.p13 chr16: 58,673,818-58,674,116 , GRCh37.p13 chr16: 58,707,722-58,708,020 SLC38A7
    nsv5184495mobile element insertion1nstd203human GRCh38 chr16: 58,682,649-58,682,659 , GRCh37.p13 chr16: 58,716,553-58,716,563 SLC38A7
    nsv5158057mobile element insertion1nstd203human GRCh38 chr16: 58,673,097-58,673,112 , GRCh37.p13 chr16: 58,707,001-58,707,016 SLC38A7
    nsv5153970mobile element insertion1nstd203human GRCh38 chr16: 58,673,091-58,673,112 , GRCh37.p13 chr16: 58,706,995-58,707,016 SLC38A7
    nsv5144812mobile element insertion1nstd203human GRCh38 chr16: 58,673,093-58,673,093 , GRCh37.p13 chr16: 58,706,997-58,706,997 SLC38A7
    nsv5143153mobile element insertion1nstd203human GRCh38 chr16: 58,673,090-58,673,149 , GRCh37.p13 chr16: 58,706,994-58,707,053 SLC38A7
    nsv5142194mobile element insertion1nstd203human GRCh38 chr16: 58,673,092-58,673,092 , GRCh37.p13 chr16: 58,706,996-58,706,996 SLC38A7
    nsv5008442copy number variation1nstd200human GRCh38 chr16: 58,658,584-58,800,395 , GRCh37.p13 chr16: 58,692,488-58,834,299 GOT2, SLC38A7, 5 more genes
    nsv4900152mobile element deletion1nstd200human GRCh38 chr16: 58,673,827-58,674,108 , GRCh37.p13 chr16: 58,707,731-58,708,012 SLC38A7
    nsv4786081mobile element deletion1nstd200human GRCh37 chr16: 58,707,731-58,708,012 , GRCh38.p12 chr16: 58,673,827-58,674,108 SLC38A7
    nsv4749427copy number variation1nstd199human GRCh37 chr16: 29,238,132-88,226,311 , GRCh38.p12 chr16: 29,226,811-88,192,705 , ITGAM, 1076 more genes
    nsv4729888copy number variation1nstd102humanUncertain significance GRCh37 chr16: 57,292,407-59,103,985 , GRCh38.p12 chr16: 57,258,495-59,070,081 HMGB3P32, DOK4, 57 more genes
    nsv4548619insertion1nstd166human GRCh37.p13 chr16: 58,697,248-58,697,248 , GRCh38.p12 chr16: 58,663,344-58,663,344 SLC38A7
    nsv4456077copy number variation1nstd102humanUncertain significance GRCh37 chr16: 53,455,650-64,006,604 , GRCh38.p12 chr16: 53,421,738-63,972,700 MT1DP, RPL23AP91, 167 more genes
    nsv4436581complex substitution1nstd102humanUncertain significance GRCh38.p12 chr16: 56,334,777-90,074,947 , GRCh37 chr16: 56,368,689-90,141,355 AARS1, AP1G1, 662 more genes
    nsv4367933copy number variation1nstd173human GRCh37 chr16: 55,822,788-62,090,267 , GRCh38.p12 chr16: 55,788,876-62,056,363 , RN7SL645P, 124 more genes
    nsv4332560sequence alteration1nstd166human GRCh37.p13 chr16: 57,901,049-75,540,778 , GRCh38.p12 chr16: 57,867,145-75,506,880 , AGRP, 331 more genes
    nsv4248240copy number variation1nstd166human GRCh37.p13 chr16: 58,695,000-58,716,000 , GRCh38.p12 chr16: 58,661,096-58,682,096 SLC38A7
    nsv3921269copy number variation1nstd102humanPathogenic NCBI36 chr16: 31,893,599-88,822,254 , GRCh37.p13 chr16: 31,986,098-90,294,753 , GRCh38.p12 chr16: 31,974,777-90,228,345 LOC105371237, IGHV3OR16-11, 985 more genes
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