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Items: 1 to 20 of 118

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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
    nsv7096467copy number variation1nstd102humanUncertain significance GRCh37 chr3: 46,899,734-46,904,880 , GRCh38.p12 chr3: 46,858,244-46,863,390 MYL3
    nsv7093428delins1nstd102humanUncertain significance GRCh37 chr3: 46,900,988-46,900,992 , GRCh38 chr3: 46,859,498-46,859,502 MYL3
    nsv6713511copy number variation1nstd229human GRCh38 chr3: 46,395,301-47,630,000 , GRCh37.p13 chr3: 46,436,792-47,671,490 BOLA2P2, LRRC2-AS1, 36 more genes
    nsv6712031copy number variation1nstd229human GRCh38 chr3: 46,853,473-46,855,983 , GRCh37.p13 chr3: 46,894,963-46,897,473 MYL3
    nsv6710009copy number variation1nstd229human GRCh38 chr3: 46,860,989-46,863,261 , GRCh37.p13 chr3: 46,902,479-46,904,751 MYL3
    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
    nsv6367905copy number variation1nstd223human GRCh38 chr3: 46,833,942-46,863,366 , GRCh37.p13 chr3: 46,875,432-46,904,856 MYL3, PRSS42P
    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
    nsv6134694copy number variation1nstd213human GRCh37 chr3: 46,170,000-52,140,001 , GRCh38.p12 chr3: 46,128,508-52,105,985 ACY1, AMT, 210 more genes
    nsv5888582copy number variation1nstd209human GRCh38 chr3: 46,802,705-48,210,414 , GRCh37.p13 chr3: 46,844,195-48,251,904 SNORD13P3, LOC105377074, 34 more genes
    nsv5561912sequence alteration1nstd206human GRCh38 chr3: 46,623,292-58,677,536 , GRCh37.p13 chr3: 46,664,782-58,663,263 , CDC25A, 327 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
    nsv4877503inversion1nstd200human GRCh37 chr3: 24,885,632-100,711,157 , GRCh38.p12 chr3: 24,844,141-100,992,313 , LINC00692, 1088 more genes
    nsv4674368copy number variation1nstd102humanUncertain significance GRCh37 chr3: 46,656,350-46,990,919 , GRCh38.p12 chr3: 46,614,860-46,949,429 PRSS46P, TMIE, 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
    nsv4450409copy number variation1nstd102humanUncertain significance GRCh37 chr3: 46,904,742-46,904,890 , GRCh38 chr3: 46,863,252-46,863,400 MYL3
    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
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