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Items: 1 to 20 of 104

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976348inversion1nstd209human GRCh38 chr4: 103,823,749-108,603,414 , GRCh37.p13 chr4: 104,744,906-109,524,570 , HADH, 54 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
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    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
    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
    nsv4452806copy number variation1nstd102humannot provided GRCh37 chr4: 108,641,272-109,259,781 , GRCh38.p12 chr4: 107,720,116-108,338,625 PAPSS1, CYP2U1, 8 more genes
    nsv4342697sequence alteration1nstd166human GRCh37.p13 chr4: 73,901,505-160,870,682 , GRCh38.p12 chr4: 73,035,788-159,949,530 , ADH1B, 1083 more genes
    nsv4112040copy number variation1nstd166human GRCh37.p13 chr4: 109,097,636-109,097,938 , GRCh38.p12 chr4: 108,176,480-108,176,782 LEF1-AS1
    nsv3920388copy number variation1nstd102humanPathogenic GRCh37 chr4: 97,014,044-137,331,362 , NCBI36 chr4: 97,233,067-137,550,812 , GRCh38 chr4: 96,092,893-136,410,207 MIR576, ABT1P1, 447 more genes
    nsv3920136copy number variation1nstd102humanPathogenic GRCh37 chr4: 106,699,504-111,128,029 , GRCh38 chr4: 105,778,347-110,206,873 , NCBI36 chr4: 106,918,953-111,347,478 AIMP1, SETP20, 58 more genes
    nsv3911889copy number variation1nstd102humanUncertain significance GRCh37 chr4: 109,063,823-109,532,950 , GRCh38 chr4: 108,142,667-108,611,794 , NCBI36 chr4: 109,283,272-109,752,399 LEF1, RPL34-DT, 5 more genes
    nsv3884499copy number variation1nstd102humanPathogenic GRCh37 chr4: 12,440-190,904,441 , GRCh38.p12 chr4: 12,440-189,983,286 MTND4LP29, RNU6-128P, 2341 more genes
    nsv3883791copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-190,915,650 , GRCh38.p12 chr4: 49,556-189,994,495 LOC105377343, PDGFC, 2341 more genes
    nsv3880085copy number variation2nstd102humanPathogenic GRCh37 chr4: 68,346-190,957,473 , GRCh38.p12 chr4: 68,454-190,036,318 LOC112268460, LINC02435, 2345 more genes
    nsv3876533copy number variation1nstd102humanPathogenic GRCh37 chr4: 49,450-190,963,766 , GRCh38.p12 chr4: 49,556-190,042,611 LOC100420289, LOC100131038, 2347 more genes
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