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Items: 1 to 20 of 452

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137211copy number variation1nstd102humanPathogenic GRCh37 chr10: 11,138,692-135,427,143 , GRCh38.p12 chr10: 11,096,729-133,613,639 EXOC6, VCL, 1906 more genes
    nsv7137209copy number variation1nstd102humanPathogenic GRCh37 chr10: 12,829,206-135,427,143 , GRCh38.p12 chr10: 12,787,207-133,613,639 RNU7-12P, RNU1-65P, 1876 more genes
    nsv7093801copy number variation1nstd102humanUncertain significance GRCh37 chr10: 75,671,314-79,799,964 , GRCh38.p12 chr10: 73,911,556-78,040,206 COMTD1, DUSP13B, 53 more genes
    nsv7093733copy number variation1nstd102humanUncertain significance GRCh37 chr10: 79,163,600-79,799,964 , GRCh38.p12 chr10: 77,403,842-78,040,206 POLR3A, LOC399783, 13 more genes
    nsv7093652copy number variation1nstd102humanUncertain significance GRCh37 chr10: 79,397,003-79,603,484 , GRCh38.p12 chr10: 77,637,245-77,843,726 LOC105378372, IMPDH1P5, 5 more genes
    nsv7068053inversion1nstd229human GRCh38 chr10: 77,918,936-77,919,014 , GRCh37.p13 chr10: 79,678,694-79,678,772 DLG5
    nsv7061955inversion1nstd229human GRCh38 chr10: 77,883,806-77,883,960 , GRCh37.p13 chr10: 79,643,564-79,643,718 DLG5
    nsv6897633copy number variation1nstd229human GRCh38 chr10: 77,879,810-77,882,664 , GRCh37.p13 chr10: 79,639,568-79,642,422 DLG5
    nsv6897629copy number variation1nstd229human GRCh38 chr10: 77,785,854-77,791,018 , GRCh37.p13 chr10: 79,545,612-79,550,776 DLG5
    nsv6896696copy number variation1nstd229human GRCh38 chr10: 77,861,455-77,866,338 , GRCh37.p13 chr10: 79,621,213-79,626,096 DLG5
    nsv6896521copy number variation1nstd229human GRCh38 chr10: 77,915,138-77,923,835 , GRCh37.p13 chr10: 79,674,896-79,683,593 DLG5
    nsv6894472copy number variation1nstd229human GRCh38 chr10: 77,767,301-77,999,300 , GRCh37.p13 chr10: 79,527,059-79,759,058 H2AZP5, POLR3A, 6 more genes
    nsv6893720copy number variation1nstd229human GRCh38 chr10: 76,896,077-84,570,412 , GRCh37.p13 chr10: 78,655,835-86,330,168 RNU6-129P, LOC105378392, 111 more genes
    nsv6893578copy number variation1nstd229human GRCh38 chr10: 77,315,758-77,877,555 , GRCh37.p13 chr10: 79,075,516-79,637,313 RBBP6P1, COX6CP15, 8 more genes
    nsv6892498copy number variation1nstd229human GRCh38 chr10: 77,684,283-77,884,332 , GRCh37.p13 chr10: 79,444,041-79,644,090 LOC399783, DLG5, 4 more genes
    nsv6891465copy number variation1nstd229human GRCh38 chr10: 77,810,331-77,814,170 , GRCh37.p13 chr10: 79,570,089-79,573,928 DLG5
    nsv6889793copy number variation1nstd229human GRCh38 chr10: 77,703,590-78,390,896 , GRCh37.p13 chr10: 79,463,348-80,150,653 DLG5-AS1, GNAI2P2, 14 more genes
    nsv6885392copy number variation1nstd229human GRCh38 chr10: 77,794,984-77,795,024 , GRCh37.p13 chr10: 79,554,742-79,554,782 DLG5
    nsv6885172copy number variation1nstd229human GRCh38 chr10: 77,875,809-77,885,956 , GRCh37.p13 chr10: 79,635,567-79,645,714 DLG5
    nsv6883828copy number variation1nstd229human GRCh38 chr10: 77,864,305-77,866,932 , GRCh37.p13 chr10: 79,624,063-79,626,690 DLG5
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