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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
    nsv7096805copy number variation1nstd102humanUncertain significance GRCh37 chr3: 45,435,946-49,137,751 , GRCh38.p12 chr3: 45,394,454-49,100,318 SNORA94, LIMD1-AS1, 120 more genes
    nsv6700069copy number variation1nstd229human GRCh38 chr3: 45,896,362-46,914,422 , GRCh37.p13 chr3: 45,937,854-46,955,912 LINC02009, ALS2CL, 32 more genes
    nsv6700046copy number variation1nstd229human GRCh38 chr3: 45,938,286-45,942,640 , GRCh37.p13 chr3: 45,979,778-45,984,132 FYCO1, CXCR6
    nsv6315166copy number variation1nstd102humanPathogenic GRCh37 chr3: 44,948,482-49,115,809 , GRCh38.p12 chr3: 44,906,990-49,078,376 TMEM89, TGM4, 129 more genes
    nsv5906623copy number variation1nstd209human GRCh38 chr3: 45,938,284-45,942,636 , GRCh37.p13 chr3: 45,979,776-45,984,128 CXCR6, FYCO1
    nsv5836562copy number variation1nstd209human GRCh38 chr3: 45,938,320-45,941,919 , GRCh37.p13 chr3: 45,979,812-45,983,411 FYCO1, CXCR6
    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
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4790523copy number variation1nstd200human GRCh37 chr3: 45,979,778-45,984,129 , GRCh38.p12 chr3: 45,938,286-45,942,637 CXCR6, FYCO1
    nsv4683137copy number variation1nstd102humanUncertain significance GRCh37 chr3: 45,867,806-46,063,439 , GRCh38.p12 chr3: 45,826,314-46,021,947 CXCR6, SDHDP4, 6 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
    nsv4451167copy number variation1nstd102humanUncertain significance GRCh37 chr3: 45,862,803-46,173,511 , GRCh38.p12 chr3: 45,821,311-46,132,019 NRBF2P2, LOC105377067, 7 more genes
    nsv4347762copy number variation1nstd102humanPathogenic GRCh37 chr3: 45,153,770-53,878,616 , GRCh38.p12 chr3: 45,112,278-53,844,589 UQCRC1, DHX30, 291 more genes
    nsv3955487copy number variation1nstd168human GRCh38 chr3: 45,943,670-45,952,509 , GRCh37.p13 chr3: 45,985,162-45,994,001 CXCR6, FYCO1
    nsv3921797copy number variation1nstd102humanPathogenic NCBI36 chr3: 45,896,379-50,762,357 , GRCh38 chr3: 45,879,883-50,749,922 , GRCh37 chr3: 45,921,375-50,787,353 RBM5-AS1, PRSS42P, 185 more genes
    nsv3912340copy number variation1nstd102humanLikely benign GRCh37 chr3: 45,733,423-46,319,401 , GRCh38 chr3: 45,691,931-46,277,910 , NCBI36 chr3: 45,708,427-46,294,405 LOC105377063, XCR1, 14 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
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