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Items: 1 to 20 of 137

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5717097mobile element insertion2nstd211human GRCh38 chr11: 6,992,849-6,992,849 , GRCh37.p13 chr11: 7,014,080-7,014,080 ZNF214
    nsv5697697mobile element insertion1nstd211human GRCh38 chr11: 7,007,554-7,007,554 , GRCh37.p13 chr11: 7,028,785-7,028,785 ZNF214
    nsv5539702insertion1nstd206human GRCh38 chr11: 6,992,849-6,992,885 , GRCh37.p13 chr11: 7,014,080-7,014,116 ZNF214
    nsv5409693mobile element insertion1nstd206human GRCh38 chr11: 7,007,554-7,007,605 , GRCh37.p13 chr11: 7,028,785-7,028,836 ZNF214
    nsv5373413translocation1nstd200human GRCh38 chr11: 6,992,214-6,992,214 , GRCh38 chr11: 6,993,939-6,993,939 , GRCh37.p13 chr11: 7,013,445-7,013,445 , GRCh37.p13 chr11: 7,015,170-7,015,170 ZNF214
    nsv5354693translocation1nstd200human GRCh38 chr11: 7,019,392-7,019,392 , GRCh38 chr11: 7,019,701-7,019,701 , GRCh37.p13 chr11: 7,040,932-7,040,932 , GRCh37.p13 chr11: 7,040,623-7,040,623 NLRP14, ZNF214
    nsv5339316translocation1nstd200human GRCh37 chr11: 7,040,623-7,040,623 , GRCh37 chr11: 7,040,932-7,040,932 , GRCh38.p12 chr11: 7,019,701-7,019,701 , GRCh38.p12 chr11: 7,019,392-7,019,392 NLRP14, ZNF214
    nsv5335880translocation1nstd200human GRCh37 chr11: 7,015,170-7,015,170 , GRCh37 chr11: 7,013,445-7,013,445 , GRCh38.p12 chr11: 6,992,214-6,992,214 , GRCh38.p12 chr11: 6,993,939-6,993,939 ZNF214
    nsv5195525mobile element insertion1nstd203human GRCh38 chr11: 6,992,834-6,992,849 , GRCh37.p13 chr11: 7,014,065-7,014,080 ZNF214
    nsv4768373copy number variation1nstd102humanPathogenic GRCh37 chr11: 210,300-8,664,358 , GRCh38.p12 chr11: 210,300-8,642,811 LOC107984302, STK33, 375 more genes
    nsv4751865inversion1nstd199human GRCh37 chr11: 1,620,303-71,272,233 , GRCh38.p12 chr11: 1,599,073-71,561,187 , ACP2, 1686 more genes
    nsv4741272copy number variation1nstd199human GRCh37 chr11: 3,487,146-67,605,076 , GRCh38.p12 chr11: 3,465,916-67,837,605 , DRAP1, 1535 more genes
    nsv4674879copy number variation1nstd102humanPathogenic GRCh37 chr11: 235,934-33,826,995 , GRCh38.p12 chr11: 235,934-33,805,449 BGLT3, RPL21P97, 723 more genes
    nsv4565647inversion1nstd166human GRCh37.p13 chr11: 6,776,274-9,026,287 , GRCh38.p12 chr11: 6,755,043-9,004,740 , ZNF215, 61 more genes
    nsv4555632insertion1nstd166human GRCh37.p13 chr11: 7,014,065-7,014,065 , GRCh38.p12 chr11: 6,992,834-6,992,834 ZNF214
    nsv4548710insertion1nstd166human GRCh37.p13 chr11: 7,014,032-7,014,032 , GRCh38.p12 chr11: 6,992,801-6,992,801 ZNF214
    nsv4486426mobile element insertion1nstd166human GRCh37.p13 chr11: 7,021,904-7,021,904 , GRCh38.p12 chr11: 7,000,673-7,000,673 ZNF214
    nsv4455989copy number variation1nstd102humanUncertain significance GRCh37 chr11: 6,908,898-7,058,885 , GRCh38.p12 chr11: 6,887,667-7,037,654 ZNF214, OR2D2, 5 more genes
    nsv4383358copy number variation1nstd173human GRCh37 chr11: 7,011,531-7,035,432 , GRCh38.p12 chr11: 6,990,300-7,014,201 ZNF214, ZNF215
    nsv4370152copy number variation1nstd173human GRCh37 chr11: 6,629,042-8,085,652 , GRCh38.p12 chr11: 6,607,812-8,064,105 LOC105376533, GVINP2, 48 more genes
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