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Items: 1 to 20 of 205

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5694039mobile element insertion1nstd211human GRCh38 chr6: 52,469,894-52,469,894 , GRCh37.p13 chr6: 52,334,692-52,334,692 EFHC1
    nsv5690937mobile element insertion1nstd211human GRCh38 chr6: 52,422,096-52,422,096 , GRCh37.p13 chr6: 52,286,894-52,286,894 EFHC1
    nsv5683828mobile element insertion1nstd211human GRCh38 chr6: 52,422,112-52,422,112 , GRCh37.p13 chr6: 52,286,910-52,286,910 EFHC1
    nsv5579107copy number variation1nstd207human GRCh38 chr6: 52,472,636-52,472,689 , GRCh37.p13 chr6: 52,337,434-52,337,487 EFHC1
    nsv5558551sequence alteration1nstd206human GRCh38 chr6: 40,895,286-71,029,944 , GRCh37.p13 chr6: 40,863,025-71,739,647 , ACTG1P9, 405 more genes
    nsv5462854copy number variation1nstd206human GRCh38 chr6: 52,442,129-52,442,912 , GRCh37.p13 chr6: 52,306,927-52,307,710 EFHC1
    nsv5460724copy number variation1nstd206human GRCh38 chr6: 52,376,212-52,424,955 , GRCh37.p13 chr6: 52,241,010-52,289,753 PAQR8, EFHC1
    nsv5454797copy number variation1nstd206human GRCh38 chr6: 52,419,705-52,424,781 , GRCh37.p13 chr6: 52,284,503-52,289,579 EFHC1
    nsv5411707mobile element insertion1nstd206human GRCh38 chr6: 52,469,894-52,469,945 , GRCh37.p13 chr6: 52,334,692-52,334,743 EFHC1
    nsv5395087mobile element insertion1nstd206human GRCh38 chr6: 52,422,112-52,422,163 , GRCh37.p13 chr6: 52,286,910-52,286,961 EFHC1
    nsv5381452copy number variation1nstd102humanUncertain significance GRCh37 chr6: 51,930,764-52,906,034 , GRCh38.p12 chr6: 52,065,966-53,041,236 GSTA4, LOC730101, 30 more genes
    nsv5381387copy number variation1nstd102humanUncertain significance GRCh37 chr6: 52,329,683-52,334,281 , GRCh38.p12 chr6: 52,464,885-52,469,483 EFHC1
    nsv5378463translocation1nstd200human GRCh38 chr6: 52,416,266-52,416,266 , GRCh38 chr6: 52,420,171-52,420,171 , GRCh37.p13 chr6: 52,281,064-52,281,064 , GRCh37.p13 chr6: 52,284,969-52,284,969 EFHC1
    nsv5343207translocation1nstd200human GRCh37 chr6: 52,281,064-52,281,064 , GRCh37 chr6: 52,284,969-52,284,969 , GRCh38.p12 chr6: 52,416,266-52,416,266 , GRCh38.p12 chr6: 52,420,171-52,420,171 EFHC1
    nsv5119537mobile element insertion1nstd203human GRCh38 chr6: 52,435,236-52,435,253 , GRCh37.p13 chr6: 52,300,034-52,300,051 EFHC1
    nsv5111796mobile element insertion1nstd203human GRCh38 chr6: 52,421,744-52,421,761 , GRCh37.p13 chr6: 52,286,542-52,286,559 EFHC1
    nsv4941437copy number variation1nstd200human GRCh38 chr6: 52,439,105-52,448,363 , GRCh37.p13 chr6: 52,303,903-52,313,161 EFHC1
    nsv4941436copy number variation1nstd200human GRCh38 chr6: 52,419,577-52,420,231 , GRCh37.p13 chr6: 52,284,375-52,285,029 EFHC1
    nsv4934738copy number variation1nstd200human GRCh38 chr6: 52,405,831-52,427,405 , GRCh37.p13 chr6: 52,270,629-52,292,203 PAQR8, EFHC1
    nsv4757608inversion1nstd199human GRCh37 chr6: 26,743,921-58,149,359 , GRCh38.p12 chr6: 26,823,536-61,119,912 , ABCF1, 1075 more genes
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