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Items: 1 to 20 of 949

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143920copy number variation1nstd232human GRCh37.p13 chr4: 123,936,959-123,937,007 , GRCh38.p12 chr4: 123,015,804-123,015,852 AFG2A
    nsv7097228copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 124,011,714-124,177,355 , GRCh38.p12 chr4: 123,090,559-123,256,200 AFG2A
    nsv7097227copy number variation1nstd102humanLikely pathogenic GRCh37 chr4: 123,977,522-123,978,463 , GRCh38.p12 chr4: 123,056,367-123,057,308 AFG2A
    nsv7097226copy number variation1nstd102humanPathogenic GRCh37 chr4: 123,856,849-123,978,463 , GRCh38.p12 chr4: 122,935,694-123,057,308 AFG2A, COILP2
    nsv7096978copy number variation1nstd102humanUncertain significance GRCh37 chr4: 123,868,368-124,011,880 , GRCh38.p12 chr4: 122,947,213-123,090,725 AFG2A, COILP2
    nsv7096977copy number variation1nstd102humanPathogenic GRCh37 chr4: 123,818,759-124,235,219 , GRCh38.p12 chr4: 122,897,604-123,314,064 FGF2, COILP2, 2 more genes
    nsv7096974copy number variation1nstd102humanUncertain significance GRCh37 chr4: 121,616,266-124,323,706 , GRCh38.p12 chr4: 120,695,111-123,402,551 RN7SL335P, QRFPR, 40 more genes
    nsv7055145inversion1nstd229human GRCh38 chr4: 122,954,436-122,956,957 , GRCh37.p13 chr4: 123,875,591-123,878,112 AFG2A
    nsv7051830inversion1nstd229human GRCh38 chr4: 122,021,125-125,223,020 , GRCh37.p13 chr4: 122,942,280-126,144,175 SPRY1, ANKRD50, 29 more genes
    nsv7049438inversion1nstd229human GRCh38 chr4: 123,215,944-123,258,745 , GRCh37.p13 chr4: 124,137,099-124,179,900 AFG2A
    nsv7046627inversion1nstd229human GRCh38 chr4: 123,217,319-123,217,339 , GRCh37.p13 chr4: 124,138,474-124,138,494 AFG2A
    nsv7046043inversion1nstd229human GRCh38 chr4: 121,571,489-125,148,298 , GRCh37.p13 chr4: 122,492,644-126,069,453 TRC-GCA2-1, LINC02435, 39 more genes
    nsv7045204inversion1nstd229human GRCh38 chr4: 123,222,988-123,274,671 , GRCh37.p13 chr4: 124,144,143-124,195,826 AFG2A
    nsv7043432inversion1nstd229human GRCh38 chr4: 117,041,189-125,064,058 , GRCh37.p13 chr4: 117,962,345-125,985,213 SEPTIN14P4, LINC02516, 109 more genes
    nsv7041376inversion1nstd229human GRCh38 chr4: 123,114,602-123,114,685 , GRCh37.p13 chr4: 124,035,757-124,035,840 AFG2A
    nsv7040293inversion1nstd229human GRCh38 chr4: 122,406,938-123,167,062 , GRCh37.p13 chr4: 123,328,093-124,088,217 IL21-AS1, NUDT6, 11 more genes
    nsv6758064copy number variation1nstd229human GRCh38 chr4: 122,951,344-122,959,001 , GRCh37.p13 chr4: 123,872,499-123,880,156 AFG2A
    nsv6758031copy number variation1nstd229human GRCh38 chr4: 123,037,801-123,082,200 , GRCh37.p13 chr4: 123,958,956-124,003,355 AFG2A
    nsv6757937copy number variation1nstd229human GRCh38 chr4: 122,964,714-122,968,784 , GRCh37.p13 chr4: 123,885,869-123,889,939 AFG2A
    nsv6757392copy number variation1nstd229human GRCh38 chr4: 123,073,836-123,093,322 , GRCh37.p13 chr4: 123,994,991-124,014,477 AFG2A
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