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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6713100copy number variation1nstd229human GRCh38 chr3: 15,359,925-17,364,956 , GRCh37.p13 chr3: 15,401,432-17,406,448 RNU6-1024P, COLQ, 27 more genes
    nsv6634367copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,836,340-25,357,427 , GRCh38.p12 chr3: 13,794,843-25,315,936 TMEM43, SLC6A6, 132 more genes
    nsv6628484copy number variation1nstd224human GRCh37 chr3: 16,627,187-16,640,068 , GRCh38.p12 chr3: 16,585,680-16,598,561 DAZL
    nsv6537172inversion1nstd223human GRCh38 chr3: 16,591,472-16,592,302 , GRCh37.p13 chr3: 16,632,979-16,633,809 DAZL
    nsv6368178copy number variation1nstd223human GRCh38 chr3: 16,604,401-16,605,800 , GRCh37.p13 chr3: 16,645,908-16,647,307 DAZL
    nsv6359659copy number variation1nstd223human GRCh38 chr3: 16,586,939-16,587,506 , GRCh37.p13 chr3: 16,628,446-16,629,013 DAZL
    nsv6357021copy number variation1nstd223human GRCh38 chr3: 16,601,801-16,609,300 , GRCh37.p13 chr3: 16,643,308-16,650,807 DAZL
    nsv6315249copy number variation1nstd102humanPathogenic GRCh38 chr3: 13,371,737-20,095,506 , GRCh37.p13 chr3: 13,413,237-20,136,998 RNU6-905P, PRR3P1, 99 more genes
    nsv5890923copy number variation1nstd209human GRCh38 chr3: 16,603,561-16,603,975 , GRCh37.p13 chr3: 16,645,068-16,645,482 DAZL
    nsv5447910copy number variation1nstd206human GRCh38 chr3: 16,585,750-16,585,803 , GRCh37.p13 chr3: 16,627,257-16,627,310 DAZL
    nsv5442151copy number variation1nstd206human GRCh38 chr3: 16,603,562-16,603,976 , GRCh37.p13 chr3: 16,645,069-16,645,483 DAZL
    nsv5367011translocation1nstd200human GRCh38 chr3: 16,585,269-16,585,269 , GRCh38 chr3: 16,591,144-16,591,144 , GRCh37.p13 chr3: 16,626,776-16,626,776 , GRCh37.p13 chr3: 16,632,651-16,632,651 DAZL
    nsv5367010translocation1nstd200human GRCh38 chr3: 16,569,100-16,569,100 , GRCh38 chr3: 16,598,450-16,598,450 , GRCh37.p13 chr3: 16,639,957-16,639,957 , GRCh37.p13 chr3: 16,610,607-16,610,607 DAZL
    nsv5339167translocation1nstd200human GRCh37 chr3: 16,626,776-16,626,776 , GRCh37 chr3: 16,632,651-16,632,651 , GRCh38.p12 chr3: 16,585,269-16,585,269 , GRCh38.p12 chr3: 16,591,144-16,591,144 DAZL
    nsv5335398translocation1nstd200human GRCh37 chr3: 16,639,957-16,639,957 , GRCh37 chr3: 16,610,607-16,610,607 , GRCh38.p12 chr3: 16,569,100-16,569,100 , GRCh38.p12 chr3: 16,598,450-16,598,450 DAZL
    nsv5174006mobile element insertion1nstd203human GRCh38 chr3: 16,587,175-16,587,190 , GRCh37.p13 chr3: 16,628,682-16,628,697 DAZL
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4796476copy number variation1nstd200human GRCh37 chr3: 16,645,069-16,645,483 , GRCh38.p12 chr3: 16,603,562-16,603,976 DAZL
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