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Items: 1 to 20 of 163

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5950465insertion1nstd209human GRCh38 chr7: 92,122,220-92,122,220 , GRCh37.p13 chr7: 91,751,534-91,751,534 CYP51A1
    nsv5675872mobile element insertion2nstd211human GRCh38 chr7: 92,122,238-92,122,238 , GRCh37.p13 chr7: 91,751,552-91,751,552 CYP51A1
    nsv5627189insertion1nstd207human GRCh38 chr7: 92,122,220-92,122,220 , GRCh37.p13 chr7: 91,751,534-91,751,534 CYP51A1
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5403465mobile element insertion1nstd206human GRCh38 chr7: 92,122,220-92,122,220 , GRCh37.p13 chr7: 91,751,534-91,751,534 CYP51A1
    nsv5381780copy number variation1nstd102humanPathogenic GRCh37 chr7: 87,477,185-100,333,327 , GRCh38.p12 chr7: 87,847,870-100,735,704 ARPC1A, LOC112267858, 265 more genes
    nsv5381473copy number variation1nstd102humanUncertain significance GRCh37 chr7: 91,737,798-91,739,483 , GRCh38.p12 chr7: 92,108,484-92,110,169 CYP51A1, AKAP9
    nsv5118043mobile element insertion1nstd203human GRCh38 chr7: 92,122,226-92,122,240 , GRCh37.p13 chr7: 91,751,540-91,751,554 CYP51A1
    nsv5114934mobile element insertion1nstd203human GRCh38 chr7: 92,122,223-92,122,238 , GRCh37.p13 chr7: 91,751,537-91,751,552 CYP51A1
    nsv5114047mobile element insertion1nstd203human GRCh38 chr7: 92,122,218-92,122,238 , GRCh37.p13 chr7: 91,751,532-91,751,552 CYP51A1
    nsv5111939mobile element insertion1nstd203human GRCh38 chr7: 92,122,227-92,122,235 , GRCh37.p13 chr7: 91,751,541-91,751,549 CYP51A1
    nsv5109235mobile element insertion1nstd203human GRCh38 chr7: 92,122,224-92,122,238 , GRCh37.p13 chr7: 91,751,538-91,751,552 CYP51A1
    nsv5107657mobile element insertion1nstd203human GRCh38 chr7: 92,122,221-92,122,238 , GRCh37.p13 chr7: 91,751,535-91,751,552 CYP51A1
    nsv5104817mobile element insertion1nstd203human GRCh38 chr7: 92,122,225-92,122,238 , GRCh37.p13 chr7: 91,751,539-91,751,552 CYP51A1
    nsv5102219mobile element insertion1nstd203human GRCh38 chr7: 92,122,238-92,122,238 , GRCh37.p13 chr7: 91,751,552-91,751,552 CYP51A1
    nsv5100396mobile element insertion1nstd203human GRCh38 chr7: 92,122,220-92,122,238 , GRCh37.p13 chr7: 91,751,534-91,751,552 CYP51A1
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv5029742inversion1nstd200human GRCh38 chr7: 79,688,546-147,673,588 , GRCh37.p13 chr7: 79,317,862-147,370,680 , LOC100533722, 1168 more genes
    nsv4880762inversion1nstd200human GRCh37 chr7: 79,317,862-147,370,680 , GRCh38.p12 chr7: 79,688,546-147,673,588 , RN7SKP277, 1168 more genes
    nsv4763531inversion1nstd199human GRCh37 chr7: 66,769,373-102,019,339 , GRCh38.p12 chr7: 67,304,386-102,378,892 , ACHE, 578 more genes
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