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Items: 1 to 20 of 540

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112815copy number variation1nstd102humanPathogenic GRCh37 chr18: 54,285,235-77,960,815 , GRCh38.p12 chr18: 56,618,004-80,202,932 RPL31P9, TRG-TCC5-1, 271 more genes
    nsv6112802copy number variation1nstd102humanPathogenic GRCh37 chr18: 23,626,739-78,014,976 , GRCh38.p12 chr18: 26,046,775-80,257,093 RPL9P31, LINC02582, 595 more genes
    nsv5932624copy number variation1nstd209human GRCh38 chr18: 70,306,402-70,306,512 , GRCh37.p13 chr18: 67,973,638-67,973,748 SOCS6
    nsv5929876copy number variation1nstd209human GRCh38 chr18: 70,286,412-70,288,070 , GRCh37.p13 chr18: 67,953,648-67,955,306 SOCS6
    nsv5873320copy number variation1nstd209human GRCh38 chr18: 70,286,365-70,288,114 , GRCh37.p13 chr18: 67,953,601-67,955,350 SOCS6
    nsv5594633copy number variation1nstd207human GRCh38 chr18: 70,286,412-70,288,069 , GRCh37.p13 chr18: 67,953,648-67,955,305 SOCS6
    nsv5527426copy number variation1nstd206human GRCh38 chr18: 70,296,290-70,296,444 , GRCh37.p13 chr18: 67,963,526-67,963,680 SOCS6
    nsv5523404copy number variation1nstd206human GRCh38 chr18: 70,286,412-70,288,071 , GRCh37.p13 chr18: 67,953,648-67,955,307 SOCS6
    nsv5518209copy number variation1nstd206human GRCh38 chr18: 70,306,405-70,306,513 , GRCh37.p13 chr18: 67,973,641-67,973,749 SOCS6
    nsv5514135copy number variation1nstd206human GRCh38 chr18: 62,909,528-80,261,528 , GRCh37.p13 chr18: 60,576,761-78,017,154 , SMIM21, 190 more genes
    nsv5381802copy number variation1nstd102humanPathogenic GRCh37 chr18: 51,925,586-78,010,032 , GRCh38.p12 chr18: 54,399,216-80,252,149 LOC105372200, LOC105372174, 298 more genes
    nsv5327393copy number variation1nstd204human GRCh38.p13 chr18: 70,286,412-70,288,071 , GRCh37.p13 chr18: 67,953,648-67,955,307 SOCS6
    nsv5299072copy number variation1nstd204human GRCh38.p13 chr18: 70,286,401-70,287,200 , GRCh37.p13 chr18: 67,953,637-67,954,436 SOCS6
    nsv5296753copy number variation1nstd204human GRCh38.p13 chr18: 70,285,401-70,289,700 , GRCh37.p13 chr18: 67,952,637-67,956,936 SOCS6
    nsv5295129copy number variation1nstd204human GRCh38.p13 chr18: 70,286,365-70,288,114 , GRCh37.p13 chr18: 67,953,601-67,955,350 SOCS6
    nsv5190816mobile element insertion1nstd203human GRCh38 chr18: 70,296,729-70,296,737 , GRCh37.p13 chr18: 67,963,965-67,963,973 SOCS6
    nsv5179244mobile element insertion1nstd203human GRCh38 chr18: 70,300,456-70,300,470 , GRCh37.p13 chr18: 67,967,692-67,967,706 SOCS6
    nsv5018747copy number variation1nstd200human GRCh38 chr18: 70,311,446-70,313,926 , GRCh37.p13 chr18: 67,978,682-67,981,162 SOCS6
    nsv5018746copy number variation1nstd200human GRCh38 chr18: 70,293,118-70,294,281 , GRCh37.p13 chr18: 67,960,354-67,961,517 SOCS6
    nsv5018745copy number variation1nstd200human GRCh38 chr18: 70,286,412-70,288,071 , GRCh37.p13 chr18: 67,953,648-67,955,307 SOCS6
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