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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5675206mobile element insertion1nstd211human GRCh38 chr6: 13,811,903-13,811,903 , GRCh37.p13 chr6: 13,812,135-13,812,135 MCUR1, LOC107986571
    nsv5456825copy number variation1nstd206human GRCh38 chr6: 13,804,935-13,805,213 , GRCh37.p13 chr6: 13,805,167-13,805,445 MCUR1
    nsv5456461copy number variation1nstd206human GRCh38 chr6: 13,808,146-13,811,821 , GRCh37.p13 chr6: 13,808,378-13,812,053 LOC107986571, MCUR1
    nsv5397098mobile element insertion1nstd206human GRCh38 chr6: 13,811,903-13,811,954 , GRCh37.p13 chr6: 13,812,135-13,812,186 MCUR1, LOC107986571
    nsv5099662mobile element insertion1nstd203human GRCh38 chr6: 13,793,171-13,793,171 , GRCh37.p13 chr6: 13,793,403-13,793,403 MCUR1
    nsv4932780copy number variation1nstd200human GRCh38 chr6: 13,808,146-13,811,821 , GRCh37.p13 chr6: 13,808,378-13,812,053 MCUR1, LOC107986571
    nsv4932779copy number variation1nstd200human GRCh38 chr6: 13,800,070-13,802,417 , GRCh37.p13 chr6: 13,800,302-13,802,649 MCUR1
    nsv4809765copy number variation1nstd200human GRCh37 chr6: 13,808,378-13,812,053 , GRCh38.p12 chr6: 13,808,146-13,811,821 MCUR1, LOC107986571
    nsv4675947copy number variation1nstd102humanUncertain significance GRCh37 chr6: 13,762,933-13,813,301 , GRCh38.p12 chr6: 13,762,701-13,813,069 MCUR1, LOC107986571
    nsv4598380copy number variation1nstd183human GRCh37 chr6: 13,808,375-13,812,053 , GRCh38.p12 chr6: 13,808,143-13,811,821 MCUR1, LOC107986571
    nsv4598377copy number variation1nstd183human GRCh37 chr6: 13,646,941-13,797,459 , GRCh38.p12 chr6: 13,646,709-13,797,227 RANBP9, MCUR1
    nsv4563579mobile element insertion1nstd166human GRCh37.p13 chr6: 13,810,139-13,810,139 , GRCh38.p12 chr6: 13,809,907-13,809,907 MCUR1
    nsv4488673mobile element insertion1nstd166human GRCh37.p13 chr6: 13,812,117-13,812,117 , GRCh38.p12 chr6: 13,811,885-13,811,885 MCUR1, LOC107986571
    nsv4456780copy number variation1nstd102humanPathogenic GRCh37 chr6: 156,974-23,221,621 , GRCh38.p12 chr6: 156,974-23,221,393 LOC105374960, LOC101928573, 342 more genes
    nsv4455888copy number variation1nstd102humanUncertain significance GRCh37 chr6: 13,248,587-18,083,552 , GRCh38.p12 chr6: 13,248,355-18,083,321 RNU6-522P, LOC105374942, 70 more genes
    nsv4324882inversion1nstd166human GRCh37.p13 chr6: 11,087,007-14,472,606 , GRCh38.p12 chr6: 11,086,774-14,472,375 , HIVEP1, 56 more genes
    nsv4130041copy number variation1nstd166human GRCh37.p13 chr6: 13,797,900-13,805,000 , GRCh38.p12 chr6: 13,797,668-13,804,768 MCUR1
    nsv4118087copy number variation1nstd166human GRCh37.p13 chr6: 13,783,612-13,800,351 , GRCh38.p12 chr6: 13,783,380-13,800,119 MCUR1
    nsv4115186copy number variation1nstd166human GRCh37.p13 chr6: 13,808,378-13,812,053 , GRCh38.p12 chr6: 13,808,146-13,811,821 LOC107986571, MCUR1
    nsv3924426copy number variation1nstd102humanUncertain significance GRCh37 chr6: 13,232,627-13,805,381 , GRCh38 chr6: 13,232,395-13,805,149 , NCBI36 chr6: 13,340,606-13,913,360 LOC105374936, RN7SKP204, 12 more genes
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