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Items: 1 to 20 of 283

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5979435insertion1nstd209human GRCh38 chr14: 31,049,429-31,049,429 , GRCh37.p13 chr14: 31,518,635-31,518,635 AP4S1
    nsv5935079copy number variation1nstd209human GRCh38 chr14: 31,073,370-31,074,397 , GRCh37.p13 chr14: 31,542,576-31,543,603 AP4S1
    nsv5702262mobile element insertion2nstd211human GRCh38 chr14: 31,035,576-31,035,576 , GRCh37.p13 chr14: 31,504,782-31,504,782 AP4S1
    nsv5595794copy number variation1nstd207human GRCh38 chr14: 31,073,361-31,074,062 , GRCh37.p13 chr14: 31,542,567-31,543,268 AP4S1
    nsv5584537copy number variation1nstd207human GRCh38 chr14: 31,074,236-31,074,581 , GRCh37.p13 chr14: 31,543,442-31,543,787 AP4S1
    nsv5539123insertion1nstd206human GRCh38 chr14: 31,036,985-31,037,020 , GRCh37.p13 chr14: 31,506,191-31,506,226 AP4S1
    nsv5507554copy number variation1nstd206human GRCh38 chr14: 31,070,911-31,073,341 , GRCh37.p13 chr14: 31,540,117-31,542,547 AP4S1
    nsv5429889mobile element insertion1nstd206human GRCh38 chr14: 31,035,576-31,035,602 , GRCh37.p13 chr14: 31,504,782-31,504,808 AP4S1
    nsv5423983mobile element insertion1nstd206human GRCh38 chr14: 31,083,867-31,083,918 , GRCh37.p13 chr14: 31,553,073-31,553,124 AP4S1
    nsv5381770copy number variation1nstd102humanPathogenic GRCh37 chr14: 27,450,705-31,529,481 , GRCh38.p12 chr14: 26,981,499-31,060,275 RPS27AP4, LINC00645, 43 more genes
    nsv5309471copy number variation1nstd204human GRCh38.p13 chr14: 31,035,384-31,046,123 , GRCh37.p13 chr14: 31,504,590-31,515,329 AP4S1
    nsv5301536copy number variation1nstd204human GRCh38.p13 chr14: 31,073,311-31,074,442 , GRCh37.p13 chr14: 31,542,517-31,543,648 AP4S1
    nsv5277590copy number variation1nstd204human GRCh38.p13 chr14: 31,035,401-31,037,700 , GRCh37.p13 chr14: 31,504,607-31,506,906 AP4S1
    nsv5274336copy number variation1nstd204human GRCh38.p13 chr14: 31,035,401-31,047,300 , GRCh37.p13 chr14: 31,504,607-31,516,506 AP4S1
    nsv5263939copy number variation1nstd204human GRCh38.p13 chr14: 31,035,962-31,046,486 , GRCh37.p13 chr14: 31,505,168-31,515,692 AP4S1
    nsv5157030mobile element insertion1nstd203human GRCh38 chr14: 31,083,855-31,083,867 , GRCh37.p13 chr14: 31,553,061-31,553,073 AP4S1
    nsv5153798mobile element insertion1nstd203human GRCh38 chr14: 31,073,255-31,073,304 , GRCh37.p13 chr14: 31,542,461-31,542,510 AP4S1
    nsv5150378mobile element insertion1nstd203human GRCh38 chr14: 31,036,330-31,036,330 , GRCh37.p13 chr14: 31,505,536-31,505,536 AP4S1
    nsv5147309mobile element insertion1nstd203human GRCh38 chr14: 31,036,969-31,036,985 , GRCh37.p13 chr14: 31,506,175-31,506,191 AP4S1
    nsv5143481mobile element insertion1nstd203human GRCh38 chr14: 31,035,562-31,035,576 , GRCh37.p13 chr14: 31,504,768-31,504,782 AP4S1
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