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Items: 1 to 20 of 176

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5980434copy number variation1nstd102humanLikely benign GRCh37 chr7: 66,103,230-66,104,219 , GRCh38.p12 chr7: 66,638,243-66,639,232 KCTD7
    nsv5969789inversion1nstd209human GRCh37.p13 chr7: 66,030,576-66,258,666 , GRCh38 chr7: 66,565,589-66,793,679 RABGEF1, KCTD7, 5 more genes
    nsv5862875copy number variation2nstd209human GRCh38 chr7: 66,633,264-66,657,152 , GRCh37.p13 chr7: 66,098,251-66,122,139 KCTD7, RABGEF1, 1 more genes
    nsv5690771mobile element insertion1nstd211human GRCh38 chr7: 66,636,845-66,636,845 , GRCh37.p13 chr7: 66,101,832-66,101,832 KCTD7
    nsv5689219mobile element insertion1nstd211human GRCh38 chr7: 66,631,776-66,631,776 , GRCh37.p13 chr7: 66,096,763-66,096,763 KCTD7
    nsv5562329sequence alteration1nstd206human GRCh37.p13 chr7: 66,048,031-66,225,003 , GRCh38 chr7: 66,583,044-66,760,016 RABGEF1, KCTD7, 4 more genes
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5483251copy number variation1nstd206human GRCh38 chr7: 66,635,279-66,672,889 , GRCh37.p13 chr7: 66,100,266-66,137,876 RABGEF1, KCTD7, 1 more genes
    nsv5408619mobile element insertion1nstd206human GRCh38 chr7: 66,636,845-66,636,896 , GRCh37.p13 chr7: 66,101,832-66,101,883 KCTD7
    nsv5396669mobile element insertion1nstd206human GRCh38 chr7: 66,631,776-66,631,827 , GRCh37.p13 chr7: 66,096,763-66,096,814 KCTD7
    nsv5381724copy number variation1nstd102humanPathogenic GRCh37 chr7: 66,094,052-66,104,219 , GRCh38.p12 chr7: 66,629,065-66,639,232 KCTD7
    nsv5322525inversion1nstd204human GRCh37.p13 chr7: 65,776,458-71,393,640 , GRCh38.p13 chr7: 66,311,471-71,928,655 , SKP1P1, 64 more genes
    nsv5235281copy number variation1nstd204human GRCh38.p13 chr7: 66,636,801-66,753,700 , GRCh37.p13 chr7: 66,101,788-66,218,687 RABGEF1, LOC100996437, 1 more genes
    nsv5234157copy number variation1nstd204human GRCh38.p13 chr7: 66,635,901-66,672,800 , GRCh37.p13 chr7: 66,100,888-66,137,787 RABGEF1, KCTD7, 1 more genes
    nsv5230979copy number variation1nstd204human GRCh38.p13 chr7: 66,623,830-66,660,352 , GRCh37.p13 chr7: 66,088,817-66,125,339 RABGEF1, LOC100996437, 1 more genes
    nsv5221239copy number variation1nstd204human GRCh38.p13 chr7: 66,635,323-66,641,452 , GRCh37.p13 chr7: 66,100,310-66,106,439 KCTD7
    nsv5204954mobile element deletion1nstd204human GRCh38.p13 chr7: 66,632,197-66,632,512 , GRCh37.p13 chr7: 66,097,184-66,097,499 KCTD7
    nsv5106058mobile element insertion1nstd203human GRCh38 chr7: 66,631,761-66,631,776 , GRCh37.p13 chr7: 66,096,748-66,096,763 KCTD7
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4787245mobile element deletion1nstd200human GRCh37 chr7: 66,097,193-66,097,491 , GRCh38.p12 chr7: 66,632,206-66,632,504 KCTD7
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