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Items: 1 to 20 of 213

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148211copy number variation1nstd102humanPathogenic GRCh38 chr3: 15,488,109-15,489,735 , GRCh37.p13 chr3: 15,529,616-15,531,242 COLQ
    nsv7096544copy number variation1nstd102humanPathogenic GRCh37 chr3: 15,512,023-15,687,154 , GRCh38.p12 chr3: 15,470,516-15,645,647 BTD, RN7SL110P, 3 more genes
    nsv7096543copy number variation1nstd102humanUncertain significance GRCh37 chr3: 15,493,151-15,563,132 , GRCh38.p12 chr3: 15,451,644-15,521,625 MIR4270, COLQ, 1 more genes
    nsv6717728copy number variation1nstd229human GRCh38 chr3: 15,489,707-15,492,955 , GRCh37.p13 chr3: 15,531,214-15,534,462 COLQ
    nsv6714424copy number variation1nstd229human GRCh38 chr3: 15,516,044-15,524,859 , GRCh37.p13 chr3: 15,557,551-15,566,366 COLQ
    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
    nsv6712157copy number variation1nstd229human GRCh38 chr3: 15,498,139-15,502,735 , GRCh37.p13 chr3: 15,539,646-15,544,242 COLQ
    nsv6712034copy number variation1nstd229human GRCh38 chr3: 14,670,901-15,564,100 , GRCh37.p13 chr3: 14,712,408-15,605,607 COLQ, RNU6-1024P, 22 more genes
    nsv6711315copy number variation1nstd229human GRCh38 chr3: 15,457,294-15,459,125 , GRCh37.p13 chr3: 15,498,801-15,500,632 COLQ
    nsv6710066copy number variation1nstd229human GRCh38 chr3: 15,495,097-15,500,993 , GRCh37.p13 chr3: 15,536,604-15,542,500 COLQ, MIR4270
    nsv6709867copy number variation1nstd229human GRCh38 chr3: 15,454,805-15,457,497 , GRCh37.p13 chr3: 15,496,312-15,499,004 COLQ
    nsv6708100copy number variation1nstd229human GRCh38 chr3: 15,490,901-15,496,700 , GRCh37.p13 chr3: 15,532,408-15,538,207 COLQ, MIR4270
    nsv6707461copy number variation1nstd229human GRCh38 chr3: 15,498,401-15,509,200 , GRCh37.p13 chr3: 15,539,908-15,550,707 COLQ, RN7SL110P
    nsv6703844copy number variation1nstd229human GRCh38 chr3: 15,454,884-15,462,249 , GRCh37.p13 chr3: 15,496,391-15,503,756 COLQ
    nsv6703116copy number variation1nstd229human GRCh38 chr3: 15,479,845-15,483,962 , GRCh37.p13 chr3: 15,521,352-15,525,469 COLQ
    nsv6636922copy number variation1nstd102humanUncertain significance GRCh37 chr3: 15,511,615-15,612,393 , GRCh38.p12 chr3: 15,470,108-15,570,886 MIR4270, HACL1, 2 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
    nsv6628286copy number variation1nstd224human GRCh37 chr3: 15,440,556-15,520,486 , GRCh38.p12 chr3: 15,399,049-15,478,979 METTL6, RNU6-1024P, 2 more genes
    nsv6554196inversion1nstd223human GRCh38 chr3: 15,516,882-15,517,981 , GRCh37.p13 chr3: 15,558,389-15,559,488 COLQ
    nsv6361458copy number variation1nstd223human GRCh38 chr3: 15,459,653-15,462,203 , GRCh37.p13 chr3: 15,501,160-15,503,710 COLQ
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