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Items: 1 to 20 of 94

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5613131insertion1nstd207human GRCh38 chr3: 16,537,888-16,537,888 , GRCh37.p13 chr3: 16,579,395-16,579,395 LINC00690
    nsv5608299insertion1nstd207human GRCh38 chr3: 16,538,202-16,538,202 , GRCh37.p13 chr3: 16,579,709-16,579,709 LINC00690
    nsv5351480translocation1nstd200human GRCh38 chr3: 16,535,438-16,535,438 , GRCh38 chr3: 16,535,540-16,535,540 , GRCh37.p13 chr3: 16,576,945-16,576,945 , GRCh37.p13 chr3: 16,577,047-16,577,047 LINC00690
    nsv5037434inversion1nstd200human GRCh38 chr3: 5,031,119-56,902,223 , GRCh37.p13 chr3: 5,072,804-56,936,251 , IRAK2, 925 more genes
    nsv5030975inversion1nstd200human GRCh38 chr3: 15,359,090-16,552,177 , GRCh37.p13 chr3: 15,400,597-16,593,684 , MIR563, 22 more genes
    nsv5030280inversion1nstd200human GRCh38 chr3: 3,432,416-77,775,308 , GRCh37.p13 chr3: 3,474,100-77,824,459 , BHLHE40, 1198 more genes
    nsv4924212copy number variation1nstd200human GRCh38 chr3: 16,076,014-16,572,211 , GRCh37.p13 chr3: 16,117,521-16,613,718 RFTN1, GALNT15, 5 more genes
    nsv4888770inversion1nstd200human GRCh37 chr3: 3,474,100-77,824,459 , GRCh38.p12 chr3: 3,432,416-77,775,308 , ATRIP, 1198 more genes
    nsv4760851insertion1nstd199human GRCh37 chr3: 16,579,367-16,579,367 , GRCh38.p12 chr3: 16,537,860-16,537,860 LINC00690
    nsv4596191copy number variation1nstd183human GRCh37 chr3: 16,580,617-16,589,915 , GRCh38.p12 chr3: 16,539,110-16,548,408 LINC00690
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4395889copy number variation1nstd174human GRCh37 chr3: 16,579,903-16,657,470 , GRCh38.p12 chr3: 16,538,396-16,615,963 LINC00690, DAZL
    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
    nsv3919322copy number variation1nstd102humanPathogenic GRCh38 chr3: 14,360,747-21,656,134 , GRCh37 chr3: 14,402,247-21,697,626 , NCBI36 chr3: 14,377,251-21,672,630 LOC105376988, SLC6A6, 89 more genes
    nsv3907461copy number variation1nstd102humanPathogenic GRCh38 chr3: 63,843-19,510,600 , GRCh37 chr3: 105,526-19,552,092 , NCBI36 chr3: 80,526-19,527,096 TAMM41, CYCSP11, 267 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
    nsv3904668copy number variation1nstd102humanPathogenic NCBI36 chr3: 48,914-20,350,883 , GRCh37 chr3: 73,914-20,375,879 , GRCh38 chr3: 32,241-20,334,387 C3orf20, LOC107986059, 281 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
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