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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097204copy number variation1nstd102humanUncertain significance GRCh37 chr3: 50,378,802-50,471,880 , GRCh38.p12 chr3: 50,341,371-50,434,449 TMEM115, RASSF1, 5 more genes
    nsv7097202copy number variation1nstd102humanUncertain significance GRCh37 chr3: 49,866,536-50,540,854 , GRCh38.p12 chr3: 49,829,103-50,503,423 HYAL2, MON1A, 32 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
    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
    nsv6637072copy number variation1nstd102humanUncertain significance GRCh37 chr3: 50,364,292-50,492,932 , GRCh38.p12 chr3: 50,326,861-50,455,501 RASSF1, CACNA2D2, 8 more genes
    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
    nsv6253997mobile element insertion1nstd215human GRCh38 chr3: 50,348,816-50,348,816 , GRCh37.p13 chr3: 50,386,247-50,386,247 NPRL2
    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
    nsv5690373mobile element insertion1nstd211human GRCh38 chr3: 50,347,356-50,347,356 , GRCh37.p13 chr3: 50,384,787-50,384,787 NPRL2
    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
    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
    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
    nsv4564128inversion1nstd166human GRCh37.p13 chr3: 3,474,047-77,824,459 , GRCh38.p12 chr3: 3,432,363-77,775,308 , ACY1, 1205 more genes
    nsv4409984copy number variation1nstd174human GRCh37 chr3: 50,189,901-50,476,600 , GRCh38.p12 chr3: 50,152,468-50,439,169 , RNA5SP131, 23 more genes
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