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Items: 1 to 20 of 142

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5975059inversion1nstd209human GRCh38 chr4: 75,291,674-75,384,162 , GRCh37.p13 chr4: 76,216,884-76,309,372 LINC02483
    nsv5889019copy number variation1nstd209human GRCh38 chr4: 75,285,574-75,513,967 , GRCh37.p13 chr4: 76,210,784-76,439,177 RCHY1, THAP6, 2 more genes
    nsv5840385copy number variation2nstd209human GRCh38 chr4: 75,354,428-75,355,661 , GRCh37.p13 chr4: 76,279,638-76,280,871 LINC02483
    nsv5674237copy number variation1nstd102humanPathogenic GRCh38 chr4: 51,891,814-76,009,719 , GRCh37.p13 chr4: 52,757,980-76,930,872 FTLP10, RNU6-410P, 335 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5558008sequence alteration1nstd206human GRCh38 chr4: 75,291,396-75,385,331 , GRCh37.p13 chr4: 76,216,606-76,310,541 LINC02483
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5457574copy number variation1nstd206human GRCh38 chr4: 75,340,449-75,408,160 , GRCh37.p13 chr4: 76,265,659-76,333,370 LINC02483
    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
    nsv5032677inversion1nstd200human GRCh38 chr4: 74,153,605-79,796,520 , GRCh37.p13 chr4: 75,019,322-80,717,674 , LINC01094, 104 more genes
    nsv4925816copy number variation1nstd200human GRCh38 chr4: 75,340,449-75,408,160 , GRCh37.p13 chr4: 76,265,659-76,333,370 LINC02483
    nsv4923027copy number variation1nstd200human GRCh38 chr4: 75,127,283-75,401,656 , GRCh37.p13 chr4: 76,052,493-76,326,866 LOC100506253, LINC02483
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4800264copy number variation1nstd200human GRCh37 chr4: 76,210,784-76,439,178 , GRCh38.p12 chr4: 75,285,574-75,513,968 LINC02483, RCHY1, 2 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
    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
    nsv4751554inversion1nstd199human GRCh37 chr4: 18,939-191,034,785 , GRCh38.p12 chr4: 18,939-190,113,630 , ADD1, 2434 more genes
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