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Items: 1 to 20 of 89

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5896500copy number variation1nstd209human GRCh38 chr3: 171,525,972-180,293,041 , GRCh37.p13 chr3: 171,243,761-180,010,829 , RNU6-1120P, 95 more genes
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv5033132inversion1nstd200human GRCh38 chr3: 147,205,794-180,217,342 , GRCh37.p13 chr3: 146,923,581-179,935,130 , LOC105374154, 433 more genes
    nsv4674680copy number variation1nstd102humanPathogenic GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065 RNU6-1120P, LOC105374262, 323 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
    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
    nsv3918982copy number variation1nstd102humanPathogenic GRCh37 chr3: 167,885,356-197,837,049 , NCBI36 chr3: 169,368,050-199,321,446 , GRCh38 chr3: 168,167,568-198,110,178 EIF4G1, LOC105374248, 515 more genes
    nsv3918981copy number variation1nstd102humanPathogenic GRCh37 chr3: 103,145,726-197,837,049 , GRCh38 chr3: 103,426,882-198,110,178 , NCBI36 chr3: 104,628,416-199,321,446 LINC02614, LINC02054, 1469 more genes
    nsv3918784copy number variation1nstd102humanPathogenic GRCh37 chr3: 147,160,353-178,240,319 , GRCh38 chr3: 147,442,566-178,522,531 , NCBI36 chr3: 148,643,043-179,723,013 LOC105374167, LOC105374187, 394 more genes
    nsv3918692copy number variation1nstd102humanPathogenic GRCh38 chr3: 147,521,892-198,096,565 , GRCh37 chr3: 147,239,679-197,823,436 , NCBI36 chr3: 148,722,369-199,307,833 LOC105374179, LINC02038, 785 more genes
    nsv3918149copy number variation1nstd102humanPathogenic GRCh37 chr3: 155,836,230-197,851,986 , GRCh38 chr3: 156,118,441-198,125,115 , NCBI36 chr3: 157,318,924-199,336,383 LINC02031, PCBP2P4, 647 more genes
    nsv3918066copy number variation1nstd102humanPathogenic GRCh38 chr3: 152,100,512-198,118,383 , NCBI36 chr3: 153,300,991-199,329,651 , GRCh37 chr3: 151,818,301-197,845,254 LOC105374260, LOC105374174, 696 more genes
    nsv3915163copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,677,940-172,191,359 , GRCh38 chr3: 171,960,150-172,473,569 , NCBI36 chr3: 173,160,634-173,674,053 GHSR, FNDC3B, 4 more genes
    nsv3914762copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 168,918,444-189,565,754 , GRCh37 chr3: 167,435,750-188,083,060 , GRCh38 chr3: 167,717,962-188,365,272 ACTL6A, AHSG, 325 more genes
    nsv3914686copy number variation1nstd102humanPathogenic NCBI36 chr3: 158,493,861-199,345,995 , GRCh37 chr3: 157,011,167-197,861,598 , GRCh38 chr3: 157,293,378-198,134,727 RPL34P10, LOC105374264, 625 more genes
    nsv3913128copy number variation1nstd102humanPathogenic GRCh38 chr3: 156,321,878-198,113,452 , NCBI36 chr3: 157,522,361-199,324,720 , GRCh37 chr3: 156,039,667-197,840,323 SNORA4, MTCO3P38, 644 more genes
    nsv3913042copy number variation1nstd102humanPathogenic NCBI36 chr3: 166,359,093-181,330,650 , GRCh37 chr3: 164,876,399-179,847,956 , GRCh38 chr3: 165,158,611-180,130,168 LOC105374211, MCUR1P2, 169 more genes
    nsv3912173copy number variation1nstd102humanPathogenic NCBI36 chr3: 167,337,691-199,336,383 , GRCh37 chr3: 165,854,997-197,851,986 , GRCh38 chr3: 166,137,209-198,125,115 LOC105374277, ATP11B, 540 more genes
    nsv3911904copy number variation1nstd102humanLikely pathogenic NCBI36 chr3: 173,169,094-174,331,764 , GRCh37 chr3: 171,686,400-172,849,070 , GRCh38 chr3: 171,968,610-173,131,280 ECT2, GHSR, 18 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
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