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Items: 1 to 20 of 213

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5699291mobile element insertion2nstd211human GRCh38 chr9: 94,559,533-94,559,533 , GRCh37.p13 chr9: 97,321,815-97,321,815 PCAT7, FBP2
    nsv5536164insertion1nstd206human GRCh38 chr9: 94,559,533-94,559,570 , GRCh37.p13 chr9: 97,321,815-97,321,852 FBP2, PCAT7
    nsv5473938copy number variation1nstd206human GRCh38 chr9: 94,280,000-94,576,600 , GRCh37.p13 chr9: 97,042,282-97,338,882 LOC107987023, PCAT7, 12 more genes
    nsv5372833translocation1nstd200human GRCh38 chr9: 94,581,762-94,581,762 , GRCh38 chr9: 94,581,483-94,581,483 , GRCh37.p13 chr9: 97,343,765-97,343,765 , GRCh37.p13 chr9: 97,344,044-97,344,044 FBP2
    nsv5253840copy number variation1nstd204human GRCh38.p13 chr9: 94,573,334-94,592,699 , GRCh37.p13 chr9: 97,335,616-97,354,981 FBP2
    nsv5138741mobile element insertion1nstd203human GRCh38 chr9: 94,559,524-94,559,533 , GRCh37.p13 chr9: 97,321,806-97,321,815 FBP2, PCAT7
    nsv5137506mobile element insertion1nstd203human GRCh38 chr9: 94,579,050-94,579,069 , GRCh37.p13 chr9: 97,341,332-97,341,351 FBP2
    nsv5134098mobile element insertion1nstd203human GRCh38 chr9: 94,559,520-94,559,520 , GRCh37.p13 chr9: 97,321,802-97,321,802 PCAT7, FBP2
    nsv5131292mobile element insertion1nstd203human GRCh38 chr9: 94,559,519-94,559,533 , GRCh37.p13 chr9: 97,321,801-97,321,815 PCAT7, FBP2
    nsv5124754mobile element insertion1nstd203human GRCh38 chr9: 94,559,522-94,559,533 , GRCh37.p13 chr9: 97,321,804-97,321,815 FBP2, PCAT7
    nsv4973244copy number variation1nstd200human GRCh38 chr9: 94,570,864-94,576,601 , GRCh37.p13 chr9: 97,333,146-97,338,883 FBP2
    nsv4824095copy number variation1nstd200human GRCh37 chr9: 97,333,146-97,338,883 , GRCh38.p12 chr9: 94,570,864-94,576,601 FBP2
    nsv4719926insertion1nstd186human GRCh37 chr9: 97,321,801-97,321,801 , GRCh38.p12 chr9: 94,559,519-94,559,519 FBP2, PCAT7
    nsv4684256copy number variation1nstd102humanPathogenic GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991 RPS26P37, MIR27B, 238 more genes
    nsv4684026copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 96,160,235-97,428,496 , GRCh38.p12 chr9: 93,397,953-94,666,214 FBP1, PHF2, 30 more genes
    nsv4676103copy number variation1nstd102humanPathogenic NCBI36 chr9: 95,946,863-99,986,314 , GRCh37.p13 chr9: 96,907,042-100,946,493 , GRCh38.p12 chr9: 94,144,760-98,184,211 MIR3074, LOC112268039, 108 more genes
    nsv4616612copy number variation1nstd183human GRCh37 chr9: 97,316,907-97,320,096 , GRCh38.p12 chr9: 94,554,625-94,557,814 PCAT7, FBP2
    nsv4612308copy number variation1nstd183human GRCh37 chr9: 97,334,587-97,335,064 , GRCh38.p12 chr9: 94,572,305-94,572,782 FBP2
    nsv4602234copy number variation1nstd183human GRCh37 chr9: 97,334,132-97,335,037 , GRCh38.p12 chr9: 94,571,850-94,572,755 FBP2
    nsv4602141copy number variation1nstd183human GRCh37 chr9: 97,334,132-97,335,064 , GRCh38.p12 chr9: 94,571,850-94,572,782 FBP2
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