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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098947copy number variation1nstd102humanUncertain significance GRCh38 chr5: 161,615,157-162,040,104 , GRCh37.p13 chr5: 161,042,163-161,467,110 GABRA1, GABRA6, 3 more genes
    nsv7097520copy number variation1nstd102humanUncertain significance GRCh37 chr5: 161,112,996-161,324,428 , GRCh38.p12 chr5: 161,685,990-161,897,422 GABRA6, GABRA1, 2 more genes
    nsv7097132copy number variation1nstd102humanUncertain significance GRCh37 chr5: 160,721,088-161,324,428 , GRCh38.p12 chr5: 161,294,081-161,897,422 GLRXP3, LOC105377696, 4 more genes
    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
    nsv7050328inversion1nstd229human GRCh38 chr5: 161,817,629-161,817,694 , GRCh37.p13 chr5: 161,244,635-161,244,700 LOC105377696
    nsv7040173inversion1nstd229human GRCh38 chr5: 161,553,790-164,538,923 , GRCh37.p13 chr5: 160,980,796-163,965,929 NUDCD2, LOC102724458, 23 more genes
    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
    nsv6790408copy number variation1nstd229human GRCh38 chr5: 161,827,577-161,831,419 , GRCh37.p13 chr5: 161,254,583-161,258,425 LOC105377696
    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
    nsv6636858copy number variation1nstd102humanUncertain significance GRCh37 chr5: 159,535,230-161,656,766 , GRCh38.p12 chr5: 160,108,223-162,229,760 MIR146A, SNRPEP1, 23 more genes
    nsv6414000copy number variation1nstd223human GRCh38 chr5: 161,837,331-161,837,834 , GRCh37.p13 chr5: 161,264,337-161,264,840 LOC105377696
    nsv6412402copy number variation1nstd223human GRCh38 chr5: 161,822,501-161,823,400 , GRCh37.p13 chr5: 161,249,507-161,250,406 LOC105377696
    nsv6405414copy number variation1nstd223human GRCh38 chr5: 161,843,837-161,844,538 , GRCh37.p13 chr5: 161,270,843-161,271,544 LOC105377696
    nsv6402708copy number variation1nstd223human GRCh38 chr5: 161,842,201-161,843,400 , GRCh37.p13 chr5: 161,269,207-161,270,406 LOC105377696
    nsv6398847copy number variation1nstd223human GRCh38 chr5: 161,826,301-161,828,200 , GRCh37.p13 chr5: 161,253,307-161,255,206 LOC105377696
    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
    nsv6295294copy number variation1nstd186human GRCh37 chr5: 161,266,103-161,266,984 , GRCh38.p12 chr5: 161,839,097-161,839,978 LOC105377696
    nsv6290966copy number variation1nstd102humannot provided GRCh37 chr5: 155,970,607-162,450,579 , GRCh38.p12 chr5: 156,543,597-163,023,573 C1QTNF2, MED7, 86 more genes
    nsv6265608copy number variation1nstd214human GRCh38 chr5: 161,839,787-161,839,894 , GRCh37.p13 chr5: 161,266,793-161,266,900 LOC105377696
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