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Items: 1 to 20 of 96

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5901382copy number variation1nstd209human GRCh38 chr3: 11,914,401-12,871,932 , GRCh37.p13 chr3: 11,985,024-12,913,431 SYN2, KRT18P17, 20 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
    nsv4728451copy number variation1nstd102humanUncertain significance GRCh37 chr3: 12,522,670-12,893,013 , GRCh38.p12 chr3: 12,481,171-12,851,514 RAF1, CAND2, 10 more genes
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4398775copy number variation1nstd174human GRCh37 chr3: 11,950,595-12,916,751 , GRCh38.p12 chr3: 11,909,121-12,875,252 ACTG1P12, TSEN2, 22 more genes
    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
    nsv3917079copy number variation1nstd102humanUncertain significance NCBI36 chr3: 12,504,064-13,013,825 , GRCh37 chr3: 12,529,064-13,038,825 , GRCh38 chr3: 12,487,565-12,997,325 RNU6-377P, CAND2, 16 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
    nsv3896717copy number variation1nstd102humanPathogenic NCBI36 chr3: 7,372,797-14,376,946 , GRCh37 chr3: 7,397,797-14,401,942 , GRCh38 chr3: 7,356,110-14,360,442 OGG1, VN1R20P, 134 more genes
    nsv3895908copy number variation1nstd102humanPathogenic GRCh37 chr3: 73,914-13,655,318 , NCBI36 chr3: 48,914-13,630,319 , GRCh38 chr3: 32,241-13,613,818 GRM7-AS2, LOC105376949, 180 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
    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
    nsv3885029copy number variation1nstd102humanPathogenic GRCh37 chr3: 1,897,972-19,519,085 , GRCh38.p12 chr3: 1,856,288-19,477,593 VGLL4, RHBDF1P1, 247 more genes
    nsv3883804copy number variation1nstd102humanPathogenic GRCh37 chr3: 5,173,870-16,760,262 , GRCh38.p12 chr3: 5,132,185-16,718,755 JAGN1, LOC105376944, 200 more genes
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