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Items: 1 to 20 of 278

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6714922copy number variation1nstd229human GRCh38 chr3: 18,702-21,855 , GRCh37.p13 chr3: 60,380-63,533 LINC01986
    nsv6714890copy number variation1nstd229human GRCh38 chr3: 13,516-107,262 , GRCh37.p13 chr3: 60,002-148,945 LOC107986040, LINC01986, 1 more genes
    nsv6712805copy number variation1nstd229human GRCh38 chr3: 13,369-58,349 , GRCh37.p13 chr3: 60,002-100,032 LOC105376921, LINC01986
    nsv6711256copy number variation1nstd229human GRCh38 chr3: 15,071-80,111 , GRCh37.p13 chr3: 60,002-121,794 LOC107986040, LOC105376921, 1 more genes
    nsv6710430copy number variation1nstd229human GRCh38 chr3: 13,566-59,731 , GRCh37.p13 chr3: 60,002-101,414 LINC01986, LOC105376921
    nsv6710369copy number variation1nstd229human GRCh38 chr3: 17,486-58,144 , GRCh37.p13 chr3: 60,002-99,827 LOC105376921, LINC01986
    nsv6709727copy number variation1nstd229human GRCh38 chr3: 15,343-21,450 , GRCh37.p13 chr3: 60,002-63,128 LINC01986
    nsv6707467copy number variation1nstd229human GRCh38 chr3: 22,800-270,588 , GRCh37.p13 chr3: 64,474-312,271 CHL1, LOC107986040, 4 more genes
    nsv6705264copy number variation1nstd229human GRCh38 chr3: 14,417-14,491 , GRCh37.p13 chr3: 75,273,296-75,273,369 LINC01986
    nsv6704754copy number variation1nstd229human GRCh38 chr3: 13,123-16,750 , GRCh37.p13 chr3: 75,272,002-75,275,597 LINC01986
    nsv6704638copy number variation1nstd229human GRCh38 chr3: 18,001-25,300 , GRCh37.p13 chr3: 60,002-66,974 LINC01986
    nsv6702426copy number variation1nstd229human GRCh38 chr3: 21,121-22,689 , GRCh37.p13 chr3: 62,799-64,363 LINC01986
    nsv6700965copy number variation1nstd229human GRCh38 chr3: 13,261-20,105 , GRCh37.p13 chr3: 75,272,138-75,276,881 LINC01986
    nsv6700891copy number variation1nstd229human GRCh38 chr3: 16,796-19,979 , GRCh37.p13 chr3: 60,002-61,657 LINC01986
    nsv6700413copy number variation1nstd229human GRCh38 chr3: 15,103-15,194 , GRCh37.p13 chr3: 75,273,981-75,274,072 LINC01986
    nsv6698919copy number variation1nstd229human GRCh38 chr3: 21,126-111,576 , GRCh37.p13 chr3: 62,804-153,259 LINC01986, LOC105376921, 1 more genes
    nsv6637145copy number variation1nstd102humanPathogenic GRCh37 chr3: 60,931-10,687,964 , GRCh38.p12 chr3: 19,253-10,646,279 RN7SL120P, LOC105376940, 132 more genes
    nsv6636388copy number variation1nstd102humanUncertain significance GRCh37 chr3: 61,892-3,459,560 , GRCh38.p12 chr3: 20,214-3,417,876 LINC01986, LOC105376924, 30 more genes
    nsv6636323copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,892-9,769,457 , GRCh38.p12 chr3: 20,214-9,727,773 LOC107984112, LRRN1, 92 more genes
    nsv6636296copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,892-9,899,605 , GRCh38.p12 chr3: 20,214-9,857,921 GRM7-AS1, LOC105376938, 101 more genes
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