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Items: 1 to 20 of 216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097267copy number variation3nstd102humanUncertain significance GRCh37 chr5: 175,158,654-179,263,593 , GRCh38.p12 chr5: 175,731,651-179,836,593 LOC112267937, LMAN2, 122 more genes
    nsv7096770copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,413,111-179,263,593 , GRCh38.p12 chr5|NW_016107298.1: 1-602,153 , GRCh38.p12 chr5: 178,986,110-179,836,593 HMGB3P22, MAML1, 25 more genes
    nsv7055256inversion1nstd229human GRCh38 chr5: 179,642,536-179,653,973 , GRCh37.p13 chr5: 179,069,537-179,080,974 LOC100502572, C5orf60
    nsv7054209inversion1nstd229human GRCh38 chr5: 179,637,658-179,660,095 , GRCh37.p13 chr5: 179,064,659-179,087,096 C5orf60, LOC105377763, 1 more genes
    nsv7051571inversion1nstd229human GRCh38 chr5: 179,640,328-179,654,903 , GRCh37.p13 chr5: 179,067,329-179,081,904 LOC100502572, C5orf60
    nsv7042166inversion1nstd229human GRCh38 chr5: 179,632,114-179,653,951 , GRCh37.p13 chr5: 179,059,115-179,080,952 LOC100502572, HNRNPH1, 1 more genes
    nsv6793015copy number variation1nstd229human GRCh38 chr5: 179,523,101-179,640,200 , GRCh37.p13 chr5: 178,950,102-179,067,201 PRDX2P3, HNRNPH1, 5 more genes
    nsv6781702copy number variation1nstd229human GRCh38 chr5: 179,640,734-179,643,736 , GRCh37.p13 chr5: 179,067,735-179,070,737 C5orf60
    nsv6779412copy number variation1nstd229human GRCh38 chr5: 179,640,167-179,640,679 , GRCh37.p13 chr5: 179,067,168-179,067,680 C5orf60
    nsv6636440copy number variation1nstd102humanUncertain significance GRCh37 chr5: 177,746,012-179,975,280 , GRCh38.p12 chr5: 178,319,011-180,548,280 RUFY1-AS1, RPS15AP18, 60 more genes
    nsv6636392copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,947,702-179,645,244 , GRCh38.p12 chr5: 179,520,701-180,218,244 , GRCh38.p12 chr5|NW_016107298.1: 285,253-673,059 LOC646058, LOC100289470, 26 more genes
    nsv6634369copy number variation1nstd102humanPathogenic GRCh37 chr5: 170,350,336-180,719,789 , GRCh38.p12 chr5: 170,923,332-181,292,788 GFPT2, FOXO1B, 287 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
    nsv6313896copy number variation1nstd102humanUncertain significance GRCh37 chr5: 178,860,745-179,534,363 , GRCh38.p12 chr5: 179,433,744-180,107,363 , GRCh38.p12 chr5|NW_016107298.1: 198,326-673,059 RUFY1, HNRNPH1, 27 more genes
    nsv6313755copy number variation1nstd102humanUncertain significance GRCh37 chr5: 177,954,576-180,198,875 , GRCh38.p12 chr5: 178,527,575-180,771,875 MIR340, RASGEF1C, 64 more genes
    nsv6141366copy number variation1nstd206human GRCh38 chr5: 179,635,324-179,672,000 , GRCh37.p13 chr5: 179,062,325-179,099,001 LOC105377763, LOC100502572, 1 more genes
    nsv6135399copy number variation1nstd213human GRCh37 chr5: 178,600,000-179,310,001 , GRCh38.p12 chr5: 179,172,999-179,883,001 , GRCh38.p12 chr5|NW_016107298.1: 1-648,561 SQSTM1, MAML1, 24 more genes
    nsv6135397copy number variation1nstd213human GRCh37 chr5: 176,330,000-179,310,001 , GRCh38.p12 chr5: 176,902,999-179,883,001 CANX, DBN1, 95 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
    nsv6135136copy number variation1nstd213human GRCh37 chr5: 178,930,000-179,330,001 , GRCh38.p12 chr5: 179,502,999-179,903,001 , GRCh38.p12 chr5|NW_016107298.1: 267,638-668,561 CANX, HNRNPH1, 21 more genes
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