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Items: 1 to 20 of 213

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5956611insertion1nstd209human GRCh38 chr4: 81,466,805-81,466,805 , GRCh37.p13 chr4: 82,387,959-82,387,959 RASGEF1B
    nsv5614880insertion1nstd207human GRCh38 chr4: 81,466,765-81,466,765 , GRCh37.p13 chr4: 82,387,919-82,387,919 RASGEF1B
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5458547copy number variation1nstd206human GRCh38 chr4: 81,466,772-81,466,941 , GRCh37.p13 chr4: 82,387,926-82,388,095 RASGEF1B
    nsv5457146copy number variation1nstd206human GRCh38 chr4: 81,443,973-81,445,937 , GRCh37.p13 chr4: 82,365,127-82,367,091 RASGEF1B
    nsv5345781translocation1nstd200human GRCh37 chr4: 82,356,923-82,356,923 , GRCh37 chr3: 48,533,403-48,533,403 , GRCh38.p9 chr: NaN-NaN , GRCh38.p12 chr: NaN-NaN , GRCh38.p12 chr4: 81,435,769-81,435,769 RASGEF1B
    nsv5092648mobile element insertion1nstd203human GRCh38 chr4: 81,442,980-81,442,995 , GRCh37.p13 chr4: 82,364,134-82,364,149 RASGEF1B
    nsv5040446inversion1nstd200human GRCh38 chr4: 76,223,829-89,968,114 , GRCh37.p13 chr4: 77,144,982-90,889,265 , KPNA2P1, 209 more genes
    nsv5037291inversion1nstd200human GRCh38 chr4: 74,160,096-84,998,626 , GRCh37.p13 chr4: 75,025,813-85,919,779 , LOC105377302, 175 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4925853copy number variation1nstd200human GRCh38 chr4: 81,435,621-81,588,394 , GRCh37.p13 chr4: 82,356,775-82,509,548 LOC105377306, RASGEF1B
    nsv4923251copy number variation1nstd200human GRCh38 chr4: 81,462,422-81,462,493 , GRCh37.p13 chr4: 82,383,576-82,383,647 RASGEF1B
    nsv4923250copy number variation1nstd200human GRCh38 chr4: 81,443,212-81,444,503 , GRCh37.p13 chr4: 82,364,366-82,365,657 RASGEF1B
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4761770inversion1nstd199human GRCh37 chr4: 34,988-191,015,248 , GRCh38.p12 chr4: 34,988-190,094,093 , ADD1, 2433 more genes
    nsv4758212inversion1nstd199human GRCh37 chr4: 30,775-191,019,445 , GRCh38.p12 chr4: 30,775-190,098,290 , ADD1, 2433 more genes
    nsv4756209insertion1nstd199human GRCh37 chr4: 82,387,918-82,387,918 , GRCh38.p12 chr4: 81,466,764-81,466,764 RASGEF1B
    nsv4754592inversion1nstd199human GRCh37 chr4: 27,111-191,020,337 , GRCh38.p12 chr4: 27,111-190,099,182 , ADD1, 2433 more genes
    nsv4753570inversion1nstd199human GRCh37 chr4: 19,034-191,028,414 , GRCh38.p12 chr4: 19,034-190,107,259 , ADD1, 2434 more genes
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