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Items: 1 to 20 of 118

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047569inversion1nstd229human GRCh38 chr3: 152,490,812-161,531,961 , GRCh37.p13 chr3: 152,208,601-161,249,749 RPS2P19, LOC112268450, 128 more genes
    nsv6730992copy number variation1nstd229human GRCh38 chr3: 160,672,732-160,677,906 , GRCh37.p13 chr3: 160,390,520-160,395,694 ARL14
    nsv6722478copy number variation1nstd229human GRCh38 chr3: 160,676,221-160,681,457 , GRCh37.p13 chr3: 160,394,009-160,399,245 ARL14
    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
    nsv6369229copy number variation1nstd223human GRCh38 chr3: 160,673,101-160,675,500 , GRCh37.p13 chr3: 160,390,889-160,393,288 ARL14
    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
    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
    nsv6134788copy number variation1nstd213human GRCh37 chr3: 155,010,000-169,630,001 , GRCh38.p12 chr3: 155,292,211-169,912,213 , BCHE, 171 more genes
    nsv5897053copy number variation1nstd209human GRCh38 chr3: 160,676,218-160,681,452 , GRCh37.p13 chr3: 160,394,006-160,399,240 ARL14
    nsv5835302copy number variation1nstd209human GRCh38 chr3: 160,676,194-160,681,410 , GRCh37.p13 chr3: 160,393,982-160,399,198 ARL14
    nsv5834394copy number variation1nstd209human GRCh38 chr3: 160,676,694-160,678,470 , GRCh37.p13 chr3: 160,394,482-160,396,258 ARL14
    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
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4920273copy number variation1nstd200human GRCh38 chr3: 160,676,220-160,681,453 , GRCh37.p13 chr3: 160,394,008-160,399,241 ARL14
    nsv4798230copy number variation1nstd200human GRCh37 chr3: 160,394,008-160,399,241 , GRCh38.p12 chr3: 160,676,220-160,681,453 ARL14
    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
    nsv4436220copy number variation1nstd102humanUncertain significance GRCh37 chr3: 158,567,751-160,802,139 , GRCh38.p12 chr3: 158,849,962-161,084,351 SCHIP1, KRT8P12, 29 more genes
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4327115inversion1nstd166human GRCh37.p13 chr3: 131,882,701-162,233,318 , GRCh38.p12 chr3: 132,163,857-162,515,530 , ATP1B3, 446 more genes
    nsv3919833copy number variation1nstd102humanPathogenic GRCh38 chr3: 158,141,556-172,788,324 , NCBI36 chr3: 159,342,039-173,988,808 , GRCh37 chr3: 157,859,345-172,506,114 NMD3, TRV-AAC1-1, 173 more genes
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