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Items: 1 to 20 of 232

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5904040copy number variation1nstd209human GRCh38 chr4: 84,604,639-84,604,713 , GRCh37.p13 chr4: 85,525,792-85,525,866 CDS1
    nsv5899598copy number variation1nstd209human GRCh38 chr4: 84,624,346-84,625,897 , GRCh37.p13 chr4: 85,545,499-85,547,050 CDS1
    nsv5893641copy number variation1nstd209human GRCh38 chr4: 84,608,878-84,609,206 , GRCh37.p13 chr4: 85,530,031-85,530,359 CDS1
    nsv5839500copy number variation1nstd209human GRCh38 chr4: 84,624,349-84,625,894 , GRCh37.p13 chr4: 85,545,502-85,547,047 CDS1
    nsv5686834mobile element insertion1nstd211human GRCh38 chr4: 84,616,854-84,616,854 , GRCh37.p13 chr4: 85,538,007-85,538,007 CDS1
    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
    nsv5462772copy number variation1nstd206human GRCh38 chr4: 84,608,847-84,609,207 , GRCh37.p13 chr4: 85,530,000-85,530,360 CDS1
    nsv5460589copy number variation1nstd206human GRCh38 chr4: 84,624,346-84,625,898 , GRCh37.p13 chr4: 85,545,499-85,547,051 CDS1
    nsv5396593mobile element insertion1nstd206human GRCh38 chr4: 84,616,854-84,616,905 , GRCh37.p13 chr4: 85,538,007-85,538,058 CDS1
    nsv5367642translocation1nstd200human GRCh38 chr4: 84,614,019-84,614,019 , GRCh38 chr4: 84,625,475-84,625,475 , GRCh37.p13 chr4: 85,535,172-85,535,172 , GRCh37.p13 chr4: 85,546,628-85,546,628 CDS1
    nsv5346805translocation1nstd200human GRCh38 chr4: 84,625,898-84,625,898 , GRCh38 chr4: 84,624,346-84,624,346 , GRCh37.p13 chr4: 85,545,499-85,545,499 , GRCh37.p13 chr4: 85,547,051-85,547,051 CDS1
    nsv5337158translocation1nstd200human GRCh37 chr4: 85,546,628-85,546,628 , GRCh37 chr4: 85,535,172-85,535,172 , GRCh38.p12 chr4: 84,625,475-84,625,475 , GRCh38.p12 chr4: 84,614,019-84,614,019 CDS1
    nsv5335950translocation1nstd200human GRCh37 chr4: 85,547,051-85,547,051 , GRCh37 chr4: 85,545,499-85,545,499 , GRCh38.p12 chr4: 84,624,346-84,624,346 , GRCh38.p12 chr4: 84,625,898-84,625,898 CDS1
    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
    nsv4923354copy number variation1nstd200human GRCh38 chr4: 84,587,802-84,587,868 , GRCh37.p13 chr4: 85,508,955-85,509,021 CDS1
    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
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