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Items: 1 to 20 of 299

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056410inversion1nstd229human GRCh38 chr2: 155,671,571-160,808,437 , GRCh37.p13 chr2: 156,528,083-161,664,948 LOC105373714, PKP4-AS1, 64 more genes
    nsv7053431inversion1nstd229human GRCh38 chr2: 157,134,258-157,298,108 , GRCh37.p13 chr2: 157,990,770-158,154,620 GALNT5, CDK7P1, 1 more genes
    nsv7048490inversion1nstd229human GRCh38 chr2: 156,054,444-158,055,095 , GRCh37.p13 chr2: 156,910,956-158,911,607 CYTIP, LINC01876, 23 more genes
    nsv7038090inversion1nstd229human GRCh38 chr2: 152,079,952-160,943,714 , GRCh37.p13 chr2: 152,936,466-161,800,225 , ITGB6, 105 more genes
    nsv6697043copy number variation1nstd229human GRCh38 chr2: 157,306,650-157,306,787 , GRCh37.p13 chr2: 158,163,162-158,163,299 GALNT5
    nsv6692941copy number variation1nstd229human GRCh38 chr2: 157,282,757-157,284,103 , GRCh37.p13 chr2: 158,139,269-158,140,615 GALNT5
    nsv6691731copy number variation1nstd229human GRCh38 chr2: 157,289,835-157,293,005 , GRCh37.p13 chr2: 158,146,347-158,149,517 GALNT5
    nsv6689518copy number variation1nstd229human GRCh38 chr2: 157,109,924-157,419,388 , GRCh37.p13 chr2: 157,966,436-158,275,900 RN7SKP281, CYTIP, 4 more genes
    nsv6685832copy number variation1nstd229human GRCh38 chr2: 157,262,488-157,263,280 , GRCh37.p13 chr2: 158,119,000-158,119,792 GALNT5
    nsv6683078copy number variation1nstd229human GRCh38 chr2: 154,503,385-158,170,825 , GRCh37.p13 chr2: 155,359,897-159,027,337 HEBP2P1, RNU6-436P, 48 more genes
    nsv6679833copy number variation1nstd229human GRCh38 chr2: 157,230,726-158,497,988 , GRCh37.p13 chr2: 158,087,238-159,354,500 LOC105373714, ERMN, 17 more genes
    nsv6636792copy number variation1nstd102humanUncertain significance GRCh37 chr2: 156,528,912-158,233,672 , GRCh38.p12 chr2: 155,672,400-157,377,160 RN7SKP281, HEBP2P1, 17 more genes
    nsv6353547copy number variation1nstd223human GRCh38 chr2: 157,289,835-157,293,001 , GRCh37.p13 chr2: 158,146,347-158,149,513 GALNT5
    nsv6351823copy number variation1nstd223human GRCh38 chr2: 157,309,901-157,314,000 , GRCh37.p13 chr2: 158,166,413-158,170,512 GALNT5
    nsv6351631copy number variation1nstd223human GRCh38 chr2: 157,269,685-157,270,175 , GRCh37.p13 chr2: 158,126,197-158,126,687 GALNT5
    nsv6344471copy number variation1nstd223human GRCh38 chr2: 157,313,283-157,313,895 , GRCh37.p13 chr2: 158,169,795-158,170,407 GALNT5
    nsv6339087copy number variation1nstd223human GRCh38 chr2: 157,287,417-157,288,246 , GRCh37.p13 chr2: 158,143,929-158,144,758 GALNT5
    nsv6338064copy number variation1nstd223human GRCh38 chr2: 157,262,484-157,263,275 , GRCh37.p13 chr2: 158,118,996-158,119,787 GALNT5
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6295080copy number variation1nstd186human GRCh37 chr2: 158,123,090-158,123,267 , GRCh38.p12 chr2: 157,266,578-157,266,755 GALNT5
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