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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6712467copy number variation1nstd229human GRCh38 chr3: 50,554,301-50,741,300 , GRCh37.p13 chr3: 50,591,732-50,778,731 C3orf18, DOCK3, 6 more genes
    nsv6709606copy number variation1nstd229human GRCh38 chr3: 50,306,801-50,668,900 , GRCh37.p13 chr3: 50,368,278-50,706,331 CISH, ZMYND10, 16 more genes
    nsv6706322copy number variation1nstd229human GRCh38 chr3: 50,598,601-50,605,800 , GRCh37.p13 chr3: 50,636,032-50,643,231 CISH
    nsv6700836copy number variation1nstd229human GRCh38 chr3: 48,056,801-51,204,000 , GRCh37.p13 chr3: 48,098,291-51,241,431 APEH, SLC26A6, 129 more genes
    nsv6361304copy number variation1nstd223human GRCh38 chr3: 50,604,701-50,606,200 , GRCh37.p13 chr3: 50,642,132-50,643,631 CISH
    nsv6311990copy number variation1nstd102humanPathogenic GRCh37 chr3: 49,547,968-50,685,477 , GRCh38.p12 chr3: 49,510,535-50,648,046 APEH, RNA5SP131, 52 more genes
    nsv6311798copy number variation1nstd102humanUncertain significance GRCh37 chr3: 50,540,629-50,655,235 , GRCh38.p12 chr3: 50,503,198-50,617,804 MAPKAPK3, LOC105377083, 4 more genes
    nsv6311797copy number variation1nstd102humanUncertain significance GRCh37 chr3: 50,431,520-50,685,477 , GRCh38.p12 chr3: 50,394,089-50,648,046 CACNA2D2, C3orf18, 6 more genes
    nsv6135016copy number variation1nstd213human GRCh37 chr3: 48,760,000-52,290,001 , GRCh38.p12 chr3: 48,722,567-52,255,985 ACY1, ALAS1, 128 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
    nsv5891025copy number variation1nstd209human GRCh38 chr3: 49,693,626-52,462,904 , GRCh37.p13 chr3: 49,731,059-52,496,920 , SEMA3G, 106 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
    nsv5210825copy number variation1nstd204human GRCh38.p13 chr3: 50,089,801-50,648,000 , GRCh37.p13 chr3: 50,127,234-50,685,431 C3orf18, GNAI2, 30 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
    nsv4914333copy number variation1nstd200human GRCh38 chr3: 50,554,301-50,741,244 , GRCh37.p13 chr3: 50,591,732-50,778,675 CISH, MAPKAPK3, 6 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
    nsv4793988copy number variation1nstd200human GRCh37 chr3: 50,591,732-50,778,675 , GRCh38.p12 chr3: 50,554,301-50,741,244 CISH, C3orf18, 6 more genes
    nsv4728146copy number variation1nstd102humanPathogenic GRCh37 chr3: 48,807,193-51,363,558 , GRCh38.p12 chr3: 48,769,760-51,326,127 APEH, MIR5193, 90 more genes
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