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Items: 1 to 20 of 132

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6736660copy number variation1nstd229human GRCh38 chr3: 149,137,977-149,417,965 , GRCh37.p13 chr3: 148,855,764-149,135,752 , TM4SF18, 8 more genes
    nsv6728079copy number variation1nstd229human GRCh38 chr3: 149,373,720-149,373,784 , GRCh37.p13 chr3: 149,091,507-149,091,571 TM4SF1
    nsv6722521copy number variation1nstd229human GRCh38 chr3: 149,366,685-149,378,790 , GRCh37.p13 chr3: 149,084,472-149,096,577 TM4SF1, TM4SF1-AS1
    nsv6637156copy number variation1nstd102humanPathogenic GRCh37 chr3: 116,620,308-172,042,292 , GRCh38.p12 chr3: 116,901,461-172,324,502 H1-10, AADACL2-AS1, 846 more genes
    nsv6363205copy number variation1nstd223human GRCh38 chr3: 149,364,882-149,367,286 , GRCh37.p13 chr3: 149,082,669-149,085,073 TM4SF1
    nsv6313678copy number variation1nstd102humanPathogenic GRCh37 chr3: 145,486,960-160,504,834 , GRCh38.p12 chr3: 145,769,173-160,787,046 RNU6-901P, RPL32P8, 229 more genes
    nsv6311444copy number variation1nstd102humanPathogenic GRCh37 chr3: 148,447,967-151,176,497 , GRCh38.p12 chr3: 148,730,180-151,458,709 TM4SF1, FKBP1AP4, 68 more genes
    nsv6290273copy number variation1nstd102humanPathogenic GRCh37 chr3: 142,729,607-157,921,084 , GRCh38.p12 chr3: 143,010,765-158,203,295 LINC02066, TM4SF1-AS1, 206 more genes
    nsv6290244copy number variation1nstd102humanPathogenic GRCh37 chr3: 143,439,359-165,252,122 , GRCh38.p12 chr3: 143,720,517-165,534,334 LOC102724145, C3orf80, 273 more genes
    nsv6134994copy number variation1nstd213human GRCh37 chr3: 139,490,000-150,360,001 , GRCh38.p12 chr3: 139,771,158-150,642,214 , ATP1B3, 147 more genes
    nsv5381765copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,173,683-162,494,699 , GRCh38.p12 chr3: 138,454,841-162,776,911 MBNL1-AS1, LOC107986138, 339 more genes
    nsv5352026translocation1nstd200human GRCh38 chr3: 149,367,286-149,367,286 , GRCh38 chr3: 149,364,882-149,364,882 , GRCh37.p13 chr3: 149,082,669-149,082,669 , GRCh37.p13 chr3: 149,085,073-149,085,073 TM4SF1
    nsv5331050translocation1nstd200human GRCh37 chr3: 149,085,073-149,085,073 , GRCh37 chr3: 149,082,669-149,082,669 , GRCh38.p12 chr3: 149,367,286-149,367,286 , GRCh38.p12 chr3: 149,364,882-149,364,882 TM4SF1
    nsv5320849translocation1nstd204human GRCh38.p13 chr3: 149,367,286-149,367,286 , GRCh38.p13 chr3: 149,364,882-149,364,882 , GRCh37.p13 chr3: 149,082,669-149,082,669 , GRCh37.p13 chr3: 149,085,073-149,085,073 TM4SF1
    nsv5224809copy number variation1nstd204human GRCh38.p13 chr3: 149,366,372-149,368,021 , GRCh37.p13 chr3: 149,084,159-149,085,808 TM4SF1
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4714455copy number variation1nstd195human GRCh37 chr3: 148,844,801-149,097,551 , GRCh38.p12 chr3: 149,127,014-149,379,764 , CP, 7 more genes
    nsv4684209copy number variation1nstd102humanPathogenic GRCh37 chr3: 138,145,289-162,275,610 , GRCh38.p12 chr3: 138,426,447-162,557,822 MTAPP1, PLS1, 339 more genes
    nsv4674717copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 144,053,029-150,272,658 , GRCh38.p12 chr3: 144,334,187-150,554,871 AGTR1, CP, 83 more genes
    nsv4584980copy number variation1nstd183human GRCh37 chr3: 148,854,793-149,130,499 , GRCh38.p12 chr3: 149,137,006-149,412,712 , CPHL1P, 8 more genes
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