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Items: 1 to 20 of 145

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7142613copy number variation1nstd232human GRCh37.p13 chr5: 158,697,450-158,697,531 , GRCh38.p12 chr5: 159,270,442-159,270,523 UBLCP1
    nsv7093376copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 156,786,013-162,945,369 , GRCh38.p12 chr5: 157,359,005-163,518,363 ADRA1B, CCNG1, 81 more genes
    nsv7057344inversion1nstd229human GRCh38 chr5: 158,420,376-160,356,139 , GRCh37.p13 chr5: 157,847,384-159,783,146 LINC01845, TTC1, 27 more genes
    nsv7054438inversion1nstd229human GRCh38 chr5: 158,806,124-160,433,845 , GRCh37.p13 chr5: 158,233,132-159,860,852 LINC01845, TTC1, 30 more genes
    nsv7052590inversion1nstd229human GRCh38 chr5: 154,695,187-159,271,728 , GRCh37.p13 chr5: 154,074,747-158,698,736 MRPL22, LOC105377673, 58 more genes
    nsv7043766inversion1nstd229human GRCh38 chr5: 158,447,259-160,356,138 , GRCh37.p13 chr5: 157,874,267-159,783,145 ADRA1B, LOC105377687, 27 more genes
    nsv6795873copy number variation1nstd229human GRCh38 chr5: 159,270,703-159,288,382 , GRCh37.p13 chr5: 158,697,711-158,715,390 UBLCP1
    nsv6795637copy number variation1nstd229human GRCh38 chr5: 159,268,054-159,268,114 , GRCh37.p13 chr5: 158,695,062-158,695,122 UBLCP1
    nsv6794984copy number variation1nstd229human GRCh38 chr5: 159,275,371-163,261,193 , GRCh37.p13 chr5: 158,702,379-162,688,199 LOC105377685, CCNJL, 45 more genes
    nsv6793135copy number variation1nstd229human GRCh38 chr5: 159,286,410-159,292,884 , GRCh37.p13 chr5: 158,713,418-158,719,892 UBLCP1
    nsv6787550copy number variation1nstd229human GRCh38 chr5: 159,264,934-159,265,130 , GRCh37.p13 chr5: 158,691,942-158,692,138 UBLCP1
    nsv6785894copy number variation1nstd229human GRCh38 chr5: 159,151,344-160,017,075 , GRCh37.p13 chr5: 158,578,352-159,444,082 ADRA1B, TTC1, 16 more genes
    nsv6785764copy number variation1nstd229human GRCh38 chr5: 159,241,544-159,320,193 , GRCh37.p13 chr5: 158,668,552-158,747,201 RNU4ATAC2P, IL12B, 3 more genes
    nsv6780766copy number variation1nstd229human GRCh38 chr5: 159,183,001-159,283,700 , GRCh37.p13 chr5: 158,610,009-158,710,708 UBLCP1, LOC107986468, 2 more genes
    nsv6636891copy number variation1nstd102humanPathogenic GRCh37 chr5: 150,535,183-172,906,793 , GRCh38.p12 chr5: 151,155,622-173,479,790 EFCAB9, LOC112267936, 287 more genes
    nsv6411827copy number variation1nstd223human GRCh38 chr5: 159,286,410-159,292,878 , GRCh37.p13 chr5: 158,713,418-158,719,886 UBLCP1
    nsv6404579copy number variation1nstd223human GRCh38 chr5: 159,269,301-159,270,800 , GRCh37.p13 chr5: 158,696,309-158,697,808 UBLCP1
    nsv6404531copy number variation1nstd223human GRCh38 chr5: 159,281,901-159,283,900 , GRCh37.p13 chr5: 158,708,909-158,710,908 UBLCP1
    nsv6315448copy number variation1nstd102humanPathogenic GRCh37 chr5: 149,010,383-180,719,789 , GRCh38.p12 chr5: 149,630,820-181,292,788 GRM6, MIR1229, 554 more genes
    nsv6315317copy number variation1nstd102humanUncertain significance GRCh38 chr5: 158,887,731-164,722,046 , GRCh37.p13 chr5: 158,314,739-164,149,052 LINC03000, SNRPEP1, 64 more genes
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