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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5903489copy number variation1nstd209human GRCh38 chr4: 73,440,271-73,440,327 , GRCh37.p13 chr4: 74,305,988-74,306,044 AFP
    nsv5893576copy number variation1nstd209human GRCh38 chr4: 67,920,462-75,134,545 , GRCh37.p13 chr4: 68,786,180-76,059,755 , DCK, 147 more genes
    nsv5888514copy number variation1nstd209human GRCh38 chr4: 73,446,587-73,446,650 , GRCh37.p13 chr4: 74,312,304-74,312,367 AFP
    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
    nsv5565483copy number variation1nstd207human GRCh38 chr4: 73,446,587-73,446,650 , GRCh37.p13 chr4: 74,312,304-74,312,367 AFP
    nsv5547030insertion1nstd206human GRCh38 chr4: 68,996,170-113,894,177 , GRCh37.p13 chr4: 69,861,888-114,815,333 , MIR548AH, 616 more genes
    nsv5465316copy number variation1nstd206human GRCh38 chr4: 73,447,106-73,448,396 , GRCh37.p13 chr4: 74,312,823-74,314,113 AFP
    nsv5082577mobile element insertion1nstd203human GRCh38 chr4: 73,449,963-73,449,969 , GRCh37.p13 chr4: 74,315,680-74,315,686 AFP
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4922970copy number variation1nstd200human GRCh38 chr4: 73,447,057-73,448,519 , GRCh37.p13 chr4: 74,312,774-74,314,236 AFP
    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
    nsv4734629copy number variation1nstd199human GRCh37 chr4: 74,312,338-74,312,401 , GRCh38.p12 chr4: 73,446,621-73,446,684 AFP
    nsv4729598copy number variation1nstd102humanPathogenic GRCh37 chr4: 71,412,409-87,920,784 , GRCh38.p12 chr4: 70,546,692-86,999,632 PTPN11P5, LOC643014, 244 more genes
    nsv4684100copy number variation1nstd102humanUncertain significance GRCh37 chr4: 74,275,515-74,688,555 , GRCh38.p12 chr4: 73,409,798-73,822,838 AFP, LOC107986287, 5 more genes
    nsv4674589copy number variation1nstd102humanPathogenic GRCh37 chr4: 72,680,879-86,426,232 , GRCh38.p12 chr4: 71,815,162-85,505,079 SOWAHB, FTLP9, 211 more genes
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