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Items: 1 to 20 of 938

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139867copy number variation1nstd232human GRCh37.p13 chr13: 95,848,847-95,848,915 , GRCh38.p12 chr13: 95,196,593-95,196,661 ABCC4
    nsv7098899copy number variation1nstd102humanPathogenic GRCh37 chr13: 95,675,427-105,286,434 , GRCh38.p12 chr13: 95,023,173-104,634,083 PCCA, LOC105370340, 131 more genes
    nsv7094005copy number variation1nstd102humanUncertain significance GRCh37 chr13: 93,879,710-96,443,284 , GRCh38.p12 chr13: 93,227,457-95,791,030 RNA5SP36, HNRNPA1P29, 33 more genes
    nsv7072260inversion1nstd229human GRCh38 chr13: 95,246,881-95,246,911 , GRCh37.p13 chr13: 95,899,135-95,899,165 ABCC4
    nsv7070011inversion1nstd229human GRCh38 chr13: 95,128,828-95,134,207 , GRCh37.p13 chr13: 95,781,082-95,786,461 ABCC4
    nsv7067134inversion1nstd229human GRCh38 chr13: 95,138,782-95,138,870 , GRCh37.p13 chr13: 95,791,036-95,791,124 ABCC4
    nsv7060176inversion1nstd229human GRCh38 chr13: 95,240,812-95,244,156 , GRCh37.p13 chr13: 95,893,066-95,896,410 ABCC4
    nsv7058378inversion1nstd229human GRCh38 chr13: 95,183,413-95,183,517 , GRCh37.p13 chr13: 95,835,667-95,835,771 ABCC4
    nsv6957623copy number variation1nstd229human GRCh38 chr13: 95,117,023-95,133,051 , GRCh37.p13 chr13: 95,769,277-95,785,305 ABCC4
    nsv6957542copy number variation1nstd229human GRCh38 chr13: 95,240,944-95,241,786 , GRCh37.p13 chr13: 95,893,198-95,894,040 ABCC4
    nsv6956885copy number variation1nstd229human GRCh38 chr13: 95,141,947-95,146,243 , GRCh37.p13 chr13: 95,794,201-95,798,497 ABCC4
    nsv6955591copy number variation1nstd229human GRCh38 chr13: 95,203,215-95,232,874 , GRCh37.p13 chr13: 95,855,469-95,885,128 ABCC4, SNORD13G
    nsv6955589copy number variation1nstd229human GRCh38 chr13: 95,271,778-95,500,742 , GRCh37.p13 chr13: 95,924,032-96,152,996 CLDN10, MEMO1P5, 5 more genes
    nsv6955456copy number variation1nstd229human GRCh38 chr13: 95,046,101-95,112,600 , GRCh37.p13 chr13: 95,698,355-95,764,854 ABCC4
    nsv6954064copy number variation1nstd229human GRCh38 chr13: 95,180,312-95,183,106 , GRCh37.p13 chr13: 95,832,566-95,835,360 ABCC4
    nsv6951429copy number variation1nstd229human GRCh38 chr13: 95,122,168-95,122,240 , GRCh37.p13 chr13: 95,774,422-95,774,494 ABCC4
    nsv6950694copy number variation1nstd229human GRCh38 chr13: 95,083,876-95,307,720 , GRCh37.p13 chr13: 95,736,130-95,959,974 ABCC4, SNORD13G, 1 more genes
    nsv6950487copy number variation1nstd229human GRCh38 chr13: 95,166,201-95,592,300 , GRCh37.p13 chr13: 95,818,455-96,244,554 SNORD13G, ABCC4, 7 more genes
    nsv6950321copy number variation1nstd229human GRCh38 chr13: 95,128,701-95,184,100 , GRCh37.p13 chr13: 95,780,955-95,836,354 ABCC4
    nsv6949840copy number variation1nstd229human GRCh38 chr13: 95,159,116-95,166,410 , GRCh37.p13 chr13: 95,811,370-95,818,664 ABCC4
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