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Items: 1 to 20 of 680

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148132copy number variation1nstd102humanPathogenic GRCh37 chr8: 131,138,343-143,473,913 , GRCh38.p12 chr8: 130,126,097-142,392,552 LOC107983985, MIR30DHG, 104 more genes
    nsv7076793inversion1nstd229human GRCh38 chr8: 141,477,443-141,477,566 , GRCh37.p13 chr8: 142,487,543-142,487,666 MROH5
    nsv7076080inversion1nstd229human GRCh38 chr8: 137,223,456-143,780,837 , GRCh37.p13 chr8: 138,235,699-144,743,525 LOC107986906, FAM83H, 108 more genes
    nsv7070805inversion1nstd229human GRCh38 chr8: 141,436,581-141,440,875 , GRCh37.p13 chr8: 142,446,681-142,450,975 MROH5, LOC107983985
    nsv7061615inversion1nstd229human GRCh38 chr8: 139,238,401-143,070,465 , GRCh37.p13 chr8: 140,250,644-144,151,882 PEG13, LINC01300, 63 more genes
    nsv6877271copy number variation1nstd229human GRCh38 chr8: 140,943,737-141,654,830 , GRCh37.p13 chr8: 141,953,836-142,664,930 LOC105375791, HNRNPA1P38, 16 more genes
    nsv6877252copy number variation1nstd229human GRCh38 chr8: 141,350,216-141,450,920 , GRCh37.p13 chr8: 142,360,315-142,461,020 GPR20, MROH5, 5 more genes
    nsv6875469copy number variation1nstd229human GRCh38 chr8: 141,462,865-141,463,191 , GRCh37.p13 chr8: 142,472,965-142,473,291 LOC105375789, MROH5
    nsv6872342copy number variation1nstd229human GRCh38 chr8: 141,500,732-141,506,679 , GRCh37.p13 chr8: 142,510,832-142,516,779 MROH5
    nsv6870834copy number variation1nstd229human GRCh38 chr8: 141,409,808-141,509,169 , GRCh37.p13 chr8: 142,419,908-142,519,269 LOC107983985, HNRNPA1P38, 3 more genes
    nsv6870736copy number variation1nstd229human GRCh38 chr8: 141,471,233-141,703,490 , GRCh37.p13 chr8: 142,481,333-142,713,590 MROH5, LOC105375791
    nsv6866223copy number variation1nstd229human GRCh38 chr8: 141,476,168-141,483,035 , GRCh37.p13 chr8: 142,486,268-142,493,135 MROH5
    nsv6863635copy number variation1nstd229human GRCh38 chr8: 141,455,701-141,463,700 , GRCh37.p13 chr8: 142,465,801-142,473,800 HNRNPA1P38, LOC105375789, 1 more genes
    nsv6860836copy number variation1nstd229human GRCh38 chr8: 141,430,901-141,450,600 , GRCh37.p13 chr8: 142,441,001-142,460,700 LOC107983985, PTP4A3, 2 more genes
    nsv6859650copy number variation1nstd229human GRCh38 chr8: 141,453,339-141,453,785 , GRCh37.p13 chr8: 142,463,439-142,463,885 MROH5, LOC105375789
    nsv6637926copy number variation1nstd102humanUncertain significance GRCh37 chr8: 142,309,348-143,247,742 , GRCh38.p12 chr8: 141,299,249-142,166,381 HNRNPA1P38, LOC105375791, 11 more genes
    nsv6635764copy number variation1nstd227human GRCh38.p12 chr8: 141,300,558-141,442,409 , GRCh37 chr8: 142,310,657-142,452,509 , GRCh38.p12 chr8|NT_187574.1: 1-82,401 GPR20, PTP4A3, 6 more genes
    nsv6634360copy number variation1nstd102humanPathogenic GRCh37 chr8: 68,912,432-146,295,771 , GRCh38.p12 chr8: 68,000,197-145,070,385 WASHC5, LOC100132280, 1028 more genes
    nsv6632755copy number variation1nstd224human GRCh37 chr8: 141,956,904-142,639,657 , GRCh38.p12 chr8: 140,946,805-141,629,557 PTP4A3, SLC45A4, 16 more genes
    nsv6632498copy number variation1nstd224human GRCh37 chr8: 142,458,059-142,847,158 , GRCh38.p12 chr8: 141,447,959-141,765,797 HNRNPA1P38, LOC105375791, 2 more genes
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