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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7097260copy number variation1nstd102humanPathogenic GRCh37 chr4: 84,185,352-84,406,225 , GRCh38.p12 chr4: 83,264,199-83,485,072 HPSE, COQ2, 6 more genes
    nsv7054149inversion1nstd229human GRCh38 chr4: 79,216,923-83,461,355 , GRCh37.p13 chr4: 80,138,077-84,382,508 RNU6-615P, ANTXR2, 63 more genes
    nsv6752620copy number variation1nstd229human GRCh38 chr4: 82,981,801-83,434,800 , GRCh37.p13 chr4: 83,902,954-84,355,953 COPS4, HPSE, 8 more genes
    nsv6749498copy number variation1nstd229human GRCh38 chr4: 83,421,019-83,426,155 , GRCh37.p13 chr4: 84,342,172-84,347,308 HELQ
    nsv6748141copy number variation1nstd229human GRCh38 chr4: 83,271,101-83,618,600 , GRCh37.p13 chr4: 84,192,254-84,539,753 HPSE, RPL30P5, 8 more genes
    nsv6745198copy number variation1nstd229human GRCh38 chr4: 83,442,426-83,442,652 , GRCh37.p13 chr4: 84,363,579-84,363,805 HELQ
    nsv6636962copy number variation1nstd102humanUncertain significance GRCh37 chr4: 84,142,481-84,840,424 , GRCh38.p12 chr4: 83,221,328-83,919,271 GPAT3, MRPS18C, 10 more genes
    nsv6634331copy number variation1nstd102humanPathogenic GRCh37 chr4: 84,048,377-84,744,105 , GRCh38.p12 chr4: 83,127,224-83,822,952 HPSE, SLC25A14P1, 10 more genes
    nsv6629742copy number variation1nstd224human GRCh37 chr4: 84,350,739-84,362,553 , GRCh38.p12 chr4: 83,429,586-83,441,400 HELQ
    nsv6566460inversion1nstd223human GRCh38 chr4: 83,424,775-83,425,270 , GRCh37.p13 chr4: 84,345,928-84,346,423 HELQ
    nsv6563799inversion1nstd223human GRCh38 chr4: 83,428,525-83,429,303 , GRCh37.p13 chr4: 84,349,678-84,350,456 HELQ
    nsv6558361inversion1nstd223human GRCh38 chr4: 83,411,411-83,411,710 , GRCh37.p13 chr4: 84,332,564-84,332,863 HELQ
    nsv6393651copy number variation1nstd223human GRCh38 chr4: 83,439,161-83,439,515 , GRCh37.p13 chr4: 84,360,314-84,360,668 HELQ
    nsv6392770copy number variation1nstd223human GRCh38 chr4: 83,414,162-83,414,641 , GRCh37.p13 chr4: 84,335,315-84,335,794 HELQ
    nsv6392750copy number variation1nstd223human GRCh38 chr4: 83,411,603-83,412,785 , GRCh37.p13 chr4: 84,332,756-84,333,938 HELQ
    nsv6392621copy number variation1nstd223human GRCh38 chr4: 83,125,535-84,168,784 , GRCh37.p13 chr4: 84,046,688-85,089,937 LOC105377315, COQ2, 11 more genes
    nsv6392492copy number variation1nstd223human GRCh38 chr4: 83,435,201-83,436,300 , GRCh37.p13 chr4: 84,356,354-84,357,453 HELQ
    nsv6390617copy number variation1nstd223human GRCh38 chr4: 83,421,019-83,426,152 , GRCh37.p13 chr4: 84,342,172-84,347,305 HELQ
    nsv6385214copy number variation1nstd223human GRCh38 chr4: 83,423,401-83,426,058 , GRCh37.p13 chr4: 84,344,554-84,347,211 HELQ
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