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Items: 1 to 20 of 222

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148156copy number variation1nstd102humanPathogenic GRCh38 chr6: 161,349,282-170,584,790 , GRCh37.p13 chr6: 161,770,314-170,893,878 LOC105378126, LOC107986550, 149 more genes
    nsv7137133copy number variation1nstd102humanUncertain significance GRCh37 chr6: 159,006,336-170,713,678 , GRCh38.p12 chr6: 158,585,304-170,404,590 LOC101929460, GPR31, 199 more genes
    nsv7097323copy number variation1nstd102humanPathogenic GRCh37 chr6: 167,343,076-167,453,466 , GRCh38.p12 chr6: 166,929,588-167,039,978 LOC105378120, CEP43, 3 more genes
    nsv7055126inversion1nstd229human GRCh38 chr6: 166,997,608-166,997,787 , GRCh37.p13 chr6: 167,411,096-167,411,275 MIR3939, CEP43
    nsv7039011inversion1nstd229human GRCh38 chr6: 163,643,496-167,786,105 , GRCh37.p13 chr6: 164,064,528-168,186,785 HNRNPA1P49, CCR6, 70 more genes
    nsv6636689copy number variation1nstd102humanPathogenic GRCh37 chr6: 163,181,847-170,919,482 , GRCh38.p12 chr6: 162,760,815-170,610,394 GNG5P1, LINC01558, 144 more genes
    nsv6634373copy number variation1nstd102humanPathogenic GRCh37 chr6: 163,836,226-170,893,669 , GRCh38.p12 chr6: 163,415,194-170,584,581 LOC107986547, LOC107986550, 132 more genes
    nsv6630766copy number variation1nstd224human GRCh37 chr6: 167,352,408-167,571,030 , GRCh38.p12 chr6: 166,938,920-167,157,542 CCR6, GPR31, 7 more genes
    nsv6630699copy number variation1nstd224human GRCh37 chr6: 167,343,106-167,427,045 , GRCh38.p12 chr6: 166,929,618-167,013,557 CEP43, LOC105378119, 3 more genes
    nsv6609066copy number variation1nstd223human GRCh38 chr6: 166,640,539-167,163,432 , GRCh37.p13 chr6: 167,054,027-167,576,920 LOC107986671, LOC105378119, 12 more genes
    nsv6600152copy number variation1nstd223human GRCh38 chr6: 166,997,367-166,998,078 , GRCh37.p13 chr6: 167,410,855-167,411,566 MIR3939, CEP43
    nsv6315428copy number variation1nstd102humanPathogenic GRCh37 chr6: 159,121,459-170,919,482 , GRCh38.p12 chr6: 158,700,427-170,610,394 TBP, LOC105378130, 200 more genes
    nsv6313815copy number variation1nstd102humanPathogenic GRCh37 chr6: 167,317,903-170,919,482 , GRCh38.p12 chr6: 166,904,415-170,610,394 LOC285804, LOC105378149, 91 more genes
    nsv6313793copy number variation1nstd102humanPathogenic GRCh37 chr6: 162,212,864-170,919,482 , GRCh38.p12 chr6: 161,791,832-170,610,394 LOC645468, GPR31, 148 more genes
    nsv6313745copy number variation1nstd102humanPathogenic GRCh37 chr6: 163,290,087-170,919,482 , GRCh38.p12 chr6: 162,869,055-170,610,394 HGC6.3, LOC112267970, 143 more genes
    nsv6313560copy number variation1nstd102humanPathogenic GRCh37 chr6: 161,047,873-170,919,482 , GRCh38.p12 chr6: 160,626,841-170,610,394 LOC105378142, LOC100289495, 159 more genes
    nsv6291125copy number variation1nstd102humanUncertain significance GRCh37 chr6: 167,263,995-167,774,832 , GRCh38.p12 chr6: 166,850,507-167,361,344 MIR3939, RPS6KA2-AS1, 18 more genes
    nsv6141505copy number variation1nstd206human GRCh38 chr6: 166,997,679-166,998,135 , GRCh37.p13 chr6: 167,411,167-167,411,623 MIR3939, CEP43
    nsv6135738copy number variation1nstd213human GRCh37 chr6: 166,950,000-167,790,001 , GRCh38.p12 chr6: 166,536,512-167,376,513 GPR31, TCP10L3, 22 more genes
    nsv6135500copy number variation1nstd213human GRCh37 chr6: 167,410,000-167,940,001 , GRCh38.p12 chr6: 166,996,512-167,527,809 MIR3939, LOC102724220, 18 more genes
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