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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5312882copy number variation1nstd204human GRCh37.p13 chr3: 62,796,458-62,858,711 , GRCh38.p13 chr3: 62,810,783-62,873,036 CADPS, RNU6-139P
    nsv5204504copy number variation1nstd204human GRCh38.p13 chr3: 62,810,593-62,868,762 , GRCh37.p13 chr3: 62,796,268-62,854,437 CADPS, RNU6-139P
    nsv5203259copy number variation1nstd204human GRCh38.p13 chr3: 62,810,401-62,873,000 , GRCh37.p13 chr3: 62,796,076-62,858,675 CADPS, RNU6-139P
    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
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4674813copy number variation1nstd102humanUncertain significance GRCh37 chr3: 62,206,958-63,944,889 , GRCh38.p12 chr3: 62,221,284-63,959,213 RNA5SP134, LOC105377647, 22 more genes
    nsv4674306copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,449,667-65,561,638 , GRCh38.p12 chr3: 60,463,934-65,575,963 THOC7-AS1, LOC105377647, 56 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
    nsv4452524copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,076,136-65,716,956 , GRCh38.p12 chr3: 57,042,108-65,731,281 LOC105377114, FAM107A, 110 more genes
    nsv4450340copy number variation1nstd102humanUncertain significance GRCh37 chr3: 60,844,727-63,983,596 , GRCh38.p12 chr3: 60,859,055-63,997,920 RNU2-10P, THOC7, 29 more genes
    nsv4091396copy number variation1nstd166human GRCh37.p13 chr3: 62,785,722-62,838,488 , GRCh38.p12 chr3: 62,800,047-62,852,813 RNU6-139P, CADPS
    nsv3922383copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,956,521-68,514,983 , NCBI36 chr3: 61,931,561-68,597,673 , GRCh38 chr3: 61,970,847-68,465,832 UBL5P3, PRICKLE2-DT, 73 more genes
    nsv3919181copy number variation1nstd102humanPathogenic GRCh38 chr3: 54,045,018-66,060,461 , GRCh37 chr3: 54,079,045-66,046,136 , NCBI36 chr3: 54,054,085-66,021,176 MAGI1-AS1, FEZF2, 135 more genes
    nsv3917204copy number variation1nstd102humanPathogenic GRCh38 chr3: 57,430,538-64,884,522 , NCBI36 chr3: 57,391,305-64,845,237 , GRCh37 chr3: 57,416,265-64,870,197 C3orf49, PPIAP16, 93 more genes
    nsv3916461copy number variation1nstd102humanPathogenic GRCh37 chr3: 57,174,452-90,309,110 , NCBI36 chr3: 57,149,492-90,391,800 , GRCh38 chr3: 57,140,424-90,259,960 LOC105377171, HNRNPA3P6, 323 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
    nsv3885929copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 60,526,226-63,742,930 , GRCh38.p12 chr3: 60,540,493-63,757,254 FHIT, PTPRG, 29 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
    nsv3885118copy number variation1nstd102humanUncertain significance GRCh37 chr3: 62,672,490-63,375,123 , GRCh38.p12 chr3: 62,686,815-63,389,447 RNU6-139P, CADPS, 7 more genes
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