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Items: 1 to 20 of 460

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5968909inversion1nstd209human GRCh38 chr4: 184,990,077-186,324,974 , GRCh37.p13 chr4: 185,911,231-187,246,128 SLC25A4, F11, 25 more genes
    nsv5958144insertion1nstd209human GRCh38 chr4: 185,460,992-185,460,992 , GRCh37.p13 chr4: 186,382,146-186,382,146 CCDC110
    nsv5955197insertion1nstd209human GRCh38 chr4: 185,471,340-185,471,340 , GRCh37.p13 chr4: 186,392,494-186,392,494 CCDC110, LOC105377590
    nsv5906746copy number variation1nstd209human GRCh38 chr4: 184,811,279-188,219,259 , GRCh37.p13 chr4: 185,732,433-189,140,413 , FLJ38576, 61 more genes
    nsv5838502copy number variation1nstd209human GRCh38 chr4: 185,443,931-185,445,569 , GRCh37.p13 chr4: 186,365,085-186,366,723 CCDC110, CFAP96
    nsv5684535mobile element insertion2nstd211human GRCh38 chr4: 185,461,006-185,461,006 , GRCh37.p13 chr4: 186,382,160-186,382,160 CCDC110
    nsv5635313insertion1nstd207human GRCh38 chr4: 185,460,992-185,460,992 , GRCh37.p13 chr4: 186,382,146-186,382,146 CCDC110
    nsv5629507insertion1nstd207human GRCh38 chr4: 185,471,202-185,471,202 , GRCh37.p13 chr4: 186,392,356-186,392,356 LOC105377590, CCDC110
    nsv5629026insertion1nstd207human GRCh38 chr4: 185,471,291-185,471,291 , GRCh37.p13 chr4: 186,392,445-186,392,445 CCDC110, LOC105377590
    nsv5541424insertion1nstd206human GRCh38 chr4: 185,471,220-185,471,225 , GRCh37.p13 chr4: 186,392,374-186,392,379 CCDC110, LOC105377590
    nsv5461333copy number variation1nstd206human GRCh38 chr4: 185,447,190-185,601,381 , GRCh37.p13 chr4: 186,368,344-186,522,535 LOC105377590, SORBS2, 3 more genes
    nsv5456236copy number variation1nstd206human GRCh38 chr4: 185,371,381-185,447,381 , GRCh37.p13 chr4: 186,292,535-186,368,535 UFSP2, LRP2BP, 4 more genes
    nsv5407646mobile element insertion1nstd206human GRCh38 chr4: 185,460,992-185,460,992 , GRCh37.p13 chr4: 186,382,146-186,382,146 CCDC110
    nsv5367876translocation1nstd200human GRCh38 chr4: 185,461,414-185,461,414 , GRCh38 chr4: 185,556,344-185,556,344 , GRCh37.p13 chr4: 186,477,498-186,477,498 , GRCh37.p13 chr4: 186,382,568-186,382,568 CCDC110
    nsv5237216copy number variation1nstd204human GRCh38.p13 chr4: 185,457,027-185,459,126 , GRCh37.p13 chr4: 186,378,181-186,380,280 CCDC110
    nsv5233024copy number variation1nstd204human GRCh37.p13 chr4: 186,292,655-186,367,754 , GRCh38.p13 chr4: 185,371,501-185,446,600 UFSP2, LRP2BP, 4 more genes
    nsv5200366copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 179,554,876-190,916,678 , GRCh38.p12 chr4: 178,633,722-189,995,523 SLC25A4, CASP3, 151 more genes
    nsv5098328mobile element insertion1nstd203human GRCh38 chr4: 185,460,995-185,461,006 , GRCh37.p13 chr4: 186,382,149-186,382,160 CCDC110
    nsv5097222mobile element insertion1nstd203human GRCh38 chr4: 185,460,992-185,461,006 , GRCh37.p13 chr4: 186,382,146-186,382,160 CCDC110
    nsv5095666mobile element insertion1nstd203human GRCh38 chr4: 185,443,917-185,443,964 , GRCh37.p13 chr4: 186,365,071-186,365,118 CFAP96, CCDC110
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