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Items: 1 to 20 of 716

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139263insertion1nstd232human GRCh37.p13 chr13: 38,226,812-38,226,812 , GRCh38.p12 chr13: 37,652,675-37,652,675 TRPC4
    nsv7072711inversion1nstd229human GRCh38 chr13: 37,721,651-37,721,694 , GRCh37.p13 chr13: 38,295,788-38,295,831 TRPC4
    nsv7070608inversion1nstd229human GRCh38 chr13: 37,808,702-41,386,678 , GRCh37.p13 chr13: 38,382,839-41,960,814 FREM2-AS1, SUGT1P3, 63 more genes
    nsv7058180inversion1nstd229human GRCh38 chr13: 29,278,598-37,954,955 , GRCh37.p13 chr13: 29,852,735-38,529,092 ZAR1L, HSPH1, 116 more genes
    nsv6953916copy number variation1nstd229human GRCh38 chr13: 37,750,630-37,764,539 , GRCh37.p13 chr13: 38,324,767-38,338,676 TRPC4
    nsv6952788copy number variation1nstd229human GRCh38 chr13: 37,671,091-37,746,447 , GRCh37.p13 chr13: 38,245,228-38,320,584 TRPC4
    nsv6951099copy number variation1nstd229human GRCh38 chr13: 37,669,551-37,798,707 , GRCh37.p13 chr13: 38,243,688-38,372,844 TRPC4
    nsv6951070copy number variation1nstd229human GRCh38 chr13: 37,851,222-37,858,941 , GRCh37.p13 chr13: 38,425,359-38,433,078 RNA5SP26, TRPC4
    nsv6950886copy number variation1nstd229human GRCh38 chr13: 37,821,522-37,832,256 , GRCh37.p13 chr13: 38,395,659-38,406,393 TRPC4
    nsv6946950copy number variation1nstd229human GRCh38 chr13: 37,643,668-37,646,458 , GRCh37.p13 chr13: 38,217,805-38,220,595 TRPC4
    nsv6946416copy number variation1nstd229human GRCh38 chr13: 37,814,762-37,830,340 , GRCh37.p13 chr13: 38,388,899-38,404,477 TRPC4
    nsv6945043copy number variation1nstd229human GRCh38 chr13: 37,628,276-37,630,482 , GRCh37.p13 chr13: 38,202,413-38,204,619 TRPC4
    nsv6942310copy number variation1nstd229human GRCh38 chr13: 37,834,339-37,834,388 , GRCh37.p13 chr13: 38,408,476-38,408,525 TRPC4
    nsv6938493copy number variation1nstd229human GRCh38 chr13: 37,844,301-37,853,500 , GRCh37.p13 chr13: 38,418,438-38,427,637 TRPC4, RNA5SP26
    nsv6637985copy number variation1nstd102humanUncertain significance GRCh37 chr13: 36,148,057-41,670,428 , GRCh38.p12 chr13: 35,573,920-41,096,292 RPS12P24, SPART, 86 more genes
    nsv6637238copy number variation1nstd102humanPathogenic GRCh37 chr13: 35,501,428-40,901,176 , GRCh38.p12 chr13: 34,927,291-40,327,039 CCDC169-SOHLH2, RNA5SP26, 74 more genes
    nsv6634431copy number variation1nstd102humanPathogenic GRCh37 chr13: 19,253,848-115,108,937 , GRCh38.p12 chr13: 18,679,708-114,343,462 MTUS2-AS1, LOC105370213, 1330 more genes
    nsv6621682copy number variation1nstd224human GRCh37 chr13: 38,248,380-38,318,021 , GRCh38.p12 chr13: 37,674,243-37,743,884 TRPC4
    nsv6494677copy number variation1nstd223human GRCh38 chr13: 37,794,626-37,795,227 , GRCh37.p13 chr13: 38,368,763-38,369,364 TRPC4
    nsv6494257copy number variation1nstd223human GRCh38 chr13: 37,764,601-37,770,300 , GRCh37.p13 chr13: 38,338,738-38,344,437 TRPC4
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