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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5965960insertion1nstd209human GRCh38 chr5: 126,604,274-126,604,274 , GRCh37.p13 chr5: 125,939,966-125,939,966 PHAX
    nsv5899985copy number variation1nstd209human GRCh38 chr5: 126,613,129-126,616,659 , GRCh37.p13 chr5: 125,948,821-125,952,351 PHAX
    nsv5841073copy number variation1nstd209human GRCh38 chr5: 126,616,433-126,620,254 , GRCh37.p13 chr5: 125,952,125-125,955,946 PHAX
    nsv5840775copy number variation2nstd209human GRCh38 chr5: 126,612,364-126,616,532 , GRCh37.p13 chr5: 125,948,056-125,952,224 PHAX
    nsv5840774copy number variation1nstd209human GRCh38 chr5: 126,610,864-126,612,263 , GRCh37.p13 chr5: 125,946,556-125,947,955 PHAX
    nsv5468365copy number variation1nstd206human GRCh38 chr5: 126,424,914-126,763,280 , GRCh37.p13 chr5: 125,760,606-126,098,972 PHAX, GRAMD2B, 8 more genes
    nsv5459720copy number variation1nstd206human GRCh38 chr5: 126,613,154-126,616,639 , GRCh37.p13 chr5: 125,948,846-125,952,331 PHAX
    nsv5235701copy number variation1nstd204human GRCh38.p13 chr5: 126,559,001-126,646,100 , GRCh37.p13 chr5: 125,894,693-125,981,792 SPMIP10, PHAX, 2 more genes
    nsv5085824mobile element insertion1nstd203human GRCh38 chr5: 126,620,728-126,620,757 , GRCh37.p13 chr5: 125,956,420-125,956,449 PHAX
    nsv5082806mobile element insertion1nstd203human GRCh38 chr5: 126,620,727-126,620,741 , GRCh37.p13 chr5: 125,956,419-125,956,433 PHAX
    nsv5081969mobile element insertion1nstd203human GRCh38 chr5: 126,620,734-126,620,757 , GRCh37.p13 chr5: 125,956,426-125,956,449 PHAX
    nsv5080337mobile element insertion1nstd203human GRCh38 chr5: 126,620,731-126,620,757 , GRCh37.p13 chr5: 125,956,423-125,956,449 PHAX
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5034346inversion1nstd200human GRCh38 chr5: 99,223,339-135,778,784 , GRCh37.p13 chr5: 98,559,043-135,114,473 , NUDT12, 438 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4945033copy number variation1nstd200human GRCh38 chr5: 126,572,810-126,957,739 , GRCh37.p13 chr5: 125,908,502-126,293,431 PHAX, SPMIP10, 9 more genes
    nsv4938406copy number variation1nstd200human GRCh38 chr5: 126,611,170-126,614,863 , GRCh37.p13 chr5: 125,946,862-125,950,555 PHAX
    nsv4938405copy number variation1nstd200human GRCh38 chr5: 126,605,105-126,617,711 , GRCh37.p13 chr5: 125,940,797-125,953,403 PHAX
    nsv4938404copy number variation1nstd200human GRCh38 chr5: 126,600,267-126,600,382 , GRCh37.p13 chr5: 125,935,959-125,936,074 PHAX
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
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