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Items: 1 to 20 of 134

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146191copy number variation1nstd232human GRCh37.p13 chr2: 74,594,991-74,595,096 , GRCh38.p12 chr2: 74,367,864-74,367,969 DCTN1
    nsv7146137insertion1nstd232human GRCh37.p13 chr2: 74,592,786-74,592,786 , GRCh38.p12 chr2: 74,365,659-74,365,659 DCTN1
    nsv7144498insertion1nstd232human GRCh37.p13 chr2: 74,592,368-74,592,368 , GRCh38.p12 chr2: 74,365,241-74,365,241 DCTN1
    nsv7143651insertion1nstd232human GRCh37.p13 chr2: 74,593,147-74,593,147 , GRCh38.p12 chr2: 74,366,020-74,366,020 DCTN1
    nsv7141710copy number variation1nstd232human GRCh37.p13 chr2: 74,596,340-74,596,424 , GRCh38.p12 chr2: 74,369,213-74,369,297 DCTN1
    nsv7139738copy number variation1nstd232human GRCh37.p13 chr2: 74,597,471-74,597,590 , GRCh38.p12 chr2: 74,370,344-74,370,463 DCTN1
    nsv7138880copy number variation1nstd232human GRCh37.p13 chr2: 74,593,502-74,593,584 , GRCh38.p12 chr2: 74,366,375-74,366,457 DCTN1
    nsv7098872copy number variation1nstd102humanUncertain significance GRCh37 chr2: 73,716,761-75,347,894 , GRCh38.p12 chr2: 73,489,634-75,120,768 RTKN, PCGF1, 61 more genes
    nsv7096907copy number variation2nstd102humanPathogenic GRCh37 chr2: 72,359,356-74,779,761 , GRCh38.p12 chr2: 72,132,227-74,552,634 RNU6-111P, LOC105374800, 71 more genes
    nsv7096902copy number variation3nstd102humanPathogenic GRCh37 chr2: 71,004,499-74,779,761 , GRCh38.p12 chr2: 70,777,367-74,552,634 TAF13P2, LOC107985897, 100 more genes
    nsv7096520copy number variation1nstd102humanUncertain significance GRCh37 chr2: 69,240,632-74,779,761 , GRCh38.p12 chr2: 69,013,500-74,552,634 LOC112268419, DQX1, 140 more genes
    nsv7096430copy number variation1nstd102humanUncertain significance GRCh37 chr2: 74,597,072-74,607,164 , GRCh38.p12 chr2: 74,369,945-74,380,037 DCTN1
    nsv7096429copy number variation1nstd102humanUncertain significance GRCh37 chr2: 74,588,626-74,607,164 , GRCh38.p12 chr2: 74,361,499-74,380,037 DCTN1
    nsv7039989inversion1nstd229human GRCh38 chr2: 74,303,206-79,264,856 , GRCh37.p13 chr2: 74,530,333-79,491,982 WBP1, DCTN1-AS1, 80 more genes
    nsv6695828copy number variation1nstd229human GRCh38 chr2: 74,381,079-74,381,149 , GRCh37.p13 chr2: 74,608,206-74,608,276 DCTN1
    nsv6686690copy number variation1nstd229human GRCh38 chr2: 74,366,401-74,559,400 , GRCh37.p13 chr2: 74,593,528-74,786,527 DCTN1, CCDC142, 21 more genes
    nsv6679949copy number variation1nstd229human GRCh38 chr2: 74,368,859-74,528,317 , GRCh37.p13 chr2: 74,595,986-74,755,444 LBX2, WBP1, 18 more genes
    nsv6658277copy number variation1nstd229human GRCh38 chr2: 73,985,401-74,561,400 , GRCh37.p13 chr2: 74,212,528-74,788,527 MOGS, NECAP1P2, 32 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6628141copy number variation1nstd224human GRCh37 chr2: 74,058,095-75,146,159 , GRCh38.p12 chr2: 73,830,968-74,919,032 AUP1, DCTN1, 48 more genes
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