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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv5311203copy number variation1nstd204human GRCh38.p13 chr4: 98,465,397-99,287,870 , GRCh37.p13 chr4: 99,386,548-100,209,027 TBCAP3, ADH5, 19 more genes
    nsv5239886copy number variation1nstd204human GRCh38.p13 chr4: 98,506,801-99,288,000 , GRCh37.p13 chr4: 99,427,952-100,209,157 TSPAN5, PCNAP1, 19 more genes
    nsv5230365copy number variation1nstd204human GRCh38.p13 chr4: 99,249,518-99,282,067 , GRCh37.p13 chr4: 100,170,675-100,203,224 LOC100507053, ADH1A
    nsv5162683mobile element insertion1nstd203human GRCh38 chr4: 99,280,679-99,280,692 , GRCh37.p13 chr4: 100,201,836-100,201,849 ADH1A, LOC100507053
    nsv5095826mobile element insertion1nstd203human GRCh38 chr4: 99,288,005-99,288,022 , GRCh37.p13 chr4: 100,209,162-100,209,179 LOC100507053, ADH1A
    nsv5080877mobile element insertion1nstd203human GRCh38 chr4: 99,290,009-99,290,025 , GRCh37.p13 chr4: 100,211,166-100,211,182 LOC100507053, ADH1A
    nsv5034204inversion1nstd200human GRCh38 chr4: 45,103,677-117,623,076 , GRCh37.p13 chr4: 45,105,694-118,544,231 , LOC100129728, 913 more genes
    nsv4943776copy number variation1nstd200human GRCh38 chr4: 99,283,042-99,314,697 , GRCh37.p13 chr4: 100,204,199-100,235,854 LOC100507053, ADH1B, 1 more genes
    nsv4943774copy number variation1nstd200human GRCh38 chr4: 99,180,425-99,444,855 , GRCh37.p13 chr4: 100,101,582-100,366,012 ADH1B, ADH7, 5 more genes
    nsv4943767copy number variation1nstd200human GRCh38 chr4: 98,465,400-99,287,861 , GRCh37.p13 chr4: 99,386,551-100,209,018 ADH5, TSPAN5, 19 more genes
    nsv4878267inversion1nstd200human GRCh37 chr4: 45,105,694-118,544,231 , GRCh38.p12 chr4: 45,103,677-117,623,076 , MIR367, 913 more genes
    nsv4794355copy number variation1nstd200human GRCh37 chr4: 100,101,582-100,366,012 , GRCh38.p12 chr4: 99,180,425-99,444,855 ADH1C, ADH6, 5 more genes
    nsv4794350copy number variation1nstd200human GRCh37 chr4: 99,386,551-100,209,018 , GRCh38.p12 chr4: 98,465,400-99,287,861 LOC100507053, TSPAN5, 19 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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