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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6797329copy number variation1nstd229human GRCh38 chr5: 170,308,797-170,456,558 , GRCh37.p13 chr5: 169,735,801-169,883,562 KCNIP1, KCNIP1-OT1, 3 more genes
    nsv6793960copy number variation1nstd229human GRCh38 chr5: 170,311,479-170,331,716 , GRCh37.p13 chr5: 169,738,483-169,758,720 LOC100128059, LINC01366
    nsv6792909copy number variation1nstd229human GRCh38 chr5: 170,333,470-170,333,894 , GRCh37.p13 chr5: 169,760,474-169,760,898 LINC01366
    nsv6792357copy number variation1nstd229human GRCh38 chr5: 170,322,356-170,337,273 , GRCh37.p13 chr5: 169,749,360-169,764,277 LINC01366
    nsv6785272copy number variation1nstd229human GRCh38 chr5: 170,280,099-170,345,639 , GRCh37.p13 chr5: 169,707,103-169,772,643 LCP2, LINC01366, 1 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
    nsv6636414copy number variation1nstd102humanUncertain significance GRCh37 chr5: 169,679,354-170,242,652 , GRCh38.p12 chr5: 170,252,350-170,815,648 GABRP, KCNIP1-OT1, 10 more genes
    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
    nsv6300468copy number variation1nstd186human GRCh37 chr5: 169,757,168-169,757,683 , GRCh38.p12 chr5: 170,330,164-170,330,679 LINC01366
    nsv6136095copy number variation1nstd213human GRCh37 chr5: 169,340,000-169,870,001 , GRCh38.p12 chr5: 169,912,996-170,442,997 DOCK2, FOXI1, 11 more genes
    nsv6136090copy number variation1nstd213human GRCh37 chr5: 161,030,000-172,600,001 , GRCh38.p12 chr5: 161,602,994-173,172,998 BNIP1, CCNG1, 130 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv5902584copy number variation1nstd209human GRCh38 chr5: 170,274,293-170,534,408 , GRCh37.p13 chr5: 169,701,297-169,961,412 KCNMB1, LCP2, 4 more genes
    nsv5841570copy number variation1nstd209human GRCh38 chr5: 170,297,818-170,339,447 , GRCh37.p13 chr5: 169,724,822-169,766,451 LINC01366, LOC100128059, 1 more genes
    nsv5463286copy number variation1nstd206human GRCh38 chr5: 170,330,164-170,330,679 , GRCh37.p13 chr5: 169,757,168-169,757,683 LINC01366
    nsv4815468copy number variation1nstd200human GRCh37 chr5: 169,701,302-169,961,413 , GRCh38.p12 chr5: 170,274,298-170,534,409 KCNMB1, LCP2, 4 more genes
    nsv4729368copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 166,378,793-170,174,830 , GRCh38.p12 chr5: 166,951,788-170,747,826 DOCK2, FOXI1, 38 more genes
    nsv4674945copy number variation1nstd102humanPathogenic GRCh37 chr5: 156,347,980-169,959,880 , GRCh38.p12 chr5: 156,920,969-170,532,876 LINC02227, LINC01932, 146 more genes
    nsv4578263copy number variation1nstd102humanPathogenic GRCh37 chr5: 166,420,934-173,324,844 , GRCh38.p12 chr5: 166,993,929-173,897,841 LINC01187, TENM2-AS1, 112 more genes
    nsv4522015copy number variation1nstd166human GRCh37.p13 chr5: 169,752,284-169,769,754 , GRCh38.p12 chr5: 170,325,280-170,342,750 LINC01366
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