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Items: 1 to 20 of 72

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6715349copy number variation1nstd229human GRCh38 chr3: 23,767,217-24,101,093 , GRCh37.p13 chr3: 23,808,708-24,142,584 ARL4AP4, UBE2E1-AS1, 6 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
    nsv6311966copy number variation1nstd102humanPathogenic GRCh37 chr3: 16,710,965-41,275,270 , GRCh38.p12 chr3: 16,669,458-41,233,779 LOC102724104, CRIP1P2, 291 more genes
    nsv6135011copy number variation1nstd213human GRCh37 chr3: 23,210,000-24,090,001 , GRCh38.p12 chr3: 23,168,509-24,048,510 RPL15, UBE2E1, 9 more genes
    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
    nsv4684200copy number variation1nstd102humanPathogenic GRCh37 chr3: 23,960,156-23,962,548 , NCBI36 chr3: 23,935,161-23,937,553 , GRCh38 chr3: 23,918,665-23,921,057 NKIRAS1, RPL15
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4452346copy number variation1nstd102humanPathogenic GRCh37 chr3: 19,064,852-26,448,689 , GRCh38.p12 chr3: 19,023,360-26,407,198 RPL15, SGO1, 71 more genes
    nsv3970637copy number variation1nstd168human GRCh38 chr3: 23,914,246-23,933,919 , GRCh37.p13 chr3: 23,955,737-23,975,410 RPL15, NKIRAS1
    nsv3923656copy number variation1nstd102humanPathogenic GRCh38 chr3: 11,463,328-38,919,543 , NCBI36 chr3: 11,479,802-38,936,038 , GRCh37 chr3: 11,504,802-38,961,034 RN7SL4P, TOP2B, 348 more genes
    nsv3923353copy number variation1nstd102humanPathogenic GRCh38 chr3: 19,915,382-25,537,973 , GRCh37 chr3: 19,956,874-25,579,464 , NCBI36 chr3: 19,931,878-25,554,468 RNU6-822P, UBE2E1-AS1, 52 more genes
    nsv3917790copy number variation1nstd102humanUncertain significance NCBI36 chr3: 23,420,905-24,286,976 , GRCh37 chr3: 23,445,901-24,311,972 , GRCh38 chr3: 23,404,410-24,270,481 LINC00691, NKIRAS1, 12 more genes
    nsv3905127copy number variation1nstd102humanPathogenic GRCh37 chr3: 94,991-41,423,012 , NCBI36 chr3: 69,991-41,398,016 , GRCh38 chr3: 53,308-41,381,521 LINC02022, RPL23AP43, 540 more genes
    nsv3901059copy number variation1nstd102humanPathogenic GRCh37 chr3: 73,914-30,105,699 , GRCh38 chr3: 32,241-30,064,208 , NCBI36 chr3: 48,914-30,080,703 RPL32, RPL15, 369 more genes
    nsv3892895copy number variation1nstd102humanPathogenic GRCh38 chr3: 52,266-37,148,076 , GRCh37 chr3: 93,949-37,189,567 , NCBI36 chr3: 68,949-37,164,571 RPL34P11, RNU1-96P, 452 more genes
    nsv3889228copy number variation2nstd102humanPathogenic GRCh37 chr3: 61,892-197,851,986 , GRCh38.p12 chr3: 20,214-198,125,115 NDUFB4, LOC105374108, 2876 more genes
    nsv3888298copy number variation1nstd102humanPathogenic GRCh37 chr3: 13,276,005-24,295,240 , GRCh38.p12 chr3: 13,234,505-24,253,749 NR1D2, RRBP1P2, 134 more genes
    nsv3885606copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,174-197,948,027 , GRCh38.p12 chr3: 18,496-198,221,156 RNU4-62P, SEMA3B-AS1, 2880 more genes
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