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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145972copy number variation1nstd232human GRCh37.p13 chr13: 36,806,770-36,806,860 , GRCh38.p12 chr13: 36,232,633-36,232,723 CCDC169, CCDC169-SOHLH2
    nsv7143951copy number variation1nstd232human GRCh37.p13 chr13: 36,818,914-36,818,974 , GRCh38.p12 chr13: 36,244,777-36,244,837 CCDC169, CCDC169-SOHLH2
    nsv7067125inversion1nstd229human GRCh38 chr13: 36,258,913-36,289,608 , GRCh37.p13 chr13: 36,833,050-36,863,745 RNU6-71P, CCDC169, 1 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
    nsv6956869copy number variation1nstd229human GRCh38 chr13: 36,258,742-36,261,474 , GRCh37.p13 chr13: 36,832,879-36,835,611 CCDC169-SOHLH2, CCDC169
    nsv6956229copy number variation1nstd229human GRCh38 chr13: 36,266,950-36,273,173 , GRCh37.p13 chr13: 36,841,087-36,847,310 CCDC169-SOHLH2, RNU6-71P, 1 more genes
    nsv6955104copy number variation1nstd229human GRCh38 chr13: 36,217,729-36,221,512 , GRCh37.p13 chr13: 36,791,866-36,795,649 CCDC169-SOHLH2, CCDC169
    nsv6954360copy number variation1nstd229human GRCh38 chr13: 36,276,026-36,276,253 , GRCh37.p13 chr13: 36,850,163-36,850,390 CCDC169-SOHLH2, CCDC169
    nsv6951943copy number variation1nstd229human GRCh38 chr13: 36,231,655-36,234,448 , GRCh37.p13 chr13: 36,805,792-36,808,585 CCDC169-SOHLH2, CCDC169
    nsv6951916copy number variation1nstd229human GRCh38 chr13: 36,244,799-36,244,838 , GRCh37.p13 chr13: 36,818,936-36,818,975 CCDC169, CCDC169-SOHLH2
    nsv6950072copy number variation1nstd229human GRCh38 chr13: 36,190,480-36,229,043 , GRCh37.p13 chr13: 36,764,617-36,803,180 CCDC169-SOHLH2, SOHLH2, 1 more genes
    nsv6948219copy number variation1nstd229human GRCh38 chr13: 36,226,193-36,235,668 , GRCh37.p13 chr13: 36,800,330-36,809,805 CCDC169, CCDC169-SOHLH2
    nsv6945452copy number variation1nstd229human GRCh38 chr13: 36,280,621-36,301,108 , GRCh37.p13 chr13: 36,854,758-36,875,245 CCDC169-SOHLH2, SPART, 1 more genes
    nsv6945033copy number variation1nstd229human GRCh38 chr13: 36,265,801-36,302,400 , GRCh37.p13 chr13: 36,839,938-36,876,537 CCDC169, SPART, 2 more genes
    nsv6943636copy number variation1nstd229human GRCh38 chr13: 36,232,650-36,232,724 , GRCh37.p13 chr13: 36,806,787-36,806,861 CCDC169-SOHLH2, CCDC169
    nsv6942878copy number variation1nstd229human GRCh38 chr13: 36,286,475-36,289,668 , GRCh37.p13 chr13: 36,860,612-36,863,805 CCDC169-SOHLH2, CCDC169
    nsv6942164copy number variation1nstd229human GRCh38 chr13: 36,284,585-36,287,719 , GRCh37.p13 chr13: 36,858,722-36,861,856 CCDC169-SOHLH2, CCDC169
    nsv6941603copy number variation1nstd229human GRCh38 chr13: 36,241,342-36,253,903 , GRCh37.p13 chr13: 36,815,479-36,828,040 CCDC169-SOHLH2, CCDC169
    nsv6940945copy number variation1nstd229human GRCh38 chr13: 36,257,476-36,259,976 , GRCh37.p13 chr13: 36,831,613-36,834,113 CCDC169-SOHLH2, CCDC169
    nsv6938165copy number variation1nstd229human GRCh38 chr13: 36,241,341-36,247,442 , GRCh37.p13 chr13: 36,815,478-36,821,579 CCDC169-SOHLH2, CCDC169
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