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Items: 1 to 20 of 244

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7056452inversion1nstd229human GRCh38 chr2: 113,998,818-114,011,733 , GRCh37.p13 chr2: 114,756,395-114,769,310 LINC01191
    nsv7049542inversion1nstd229human GRCh38 chr2: 113,981,224-113,987,067 , GRCh37.p13 chr2: 114,738,801-114,744,644 LINC01191
    nsv7047201inversion1nstd229human GRCh38 chr2: 113,135,467-114,194,806 , GRCh37.p13 chr2: 113,893,044-114,952,383 SLC35F5, ACRP1, 26 more genes
    nsv7044064inversion1nstd229human GRCh38 chr2: 112,019,946-120,004,832 , GRCh37.p13 chr2: 112,777,523-120,762,408 LOC105373563, IL1A, 112 more genes
    nsv7042586inversion1nstd229human GRCh38 chr2: 111,572,275-118,829,502 , GRCh37.p13 chr2: 112,329,852-119,587,078 LOC105373579, NT5DC4, 103 more genes
    nsv6696373copy number variation1nstd229human GRCh38 chr2: 113,980,412-113,989,221 , GRCh37.p13 chr2: 114,737,989-114,746,798 LINC02992, LINC01191
    nsv6696361copy number variation1nstd229human GRCh38 chr2: 113,979,620-113,981,226 , GRCh37.p13 chr2: 114,737,197-114,738,803 LINC02992, LINC01191
    nsv6696313copy number variation1nstd229human GRCh38 chr2: 113,993,023-114,012,295 , GRCh37.p13 chr2: 114,750,600-114,769,872 LINC01191
    nsv6696208copy number variation1nstd229human GRCh38 chr2: 113,965,852-113,970,552 , GRCh37.p13 chr2: 114,723,429-114,728,129 LINC01191
    nsv6694528copy number variation1nstd229human GRCh38 chr2: 113,958,101-114,114,200 , GRCh37.p13 chr2: 114,715,678-114,871,777 ACTR3, LINC02992, 1 more genes
    nsv6691603copy number variation1nstd229human GRCh38 chr2: 113,985,065-114,022,227 , GRCh37.p13 chr2: 114,742,642-114,779,804 LINC01191
    nsv6686565copy number variation1nstd229human GRCh38 chr2: 113,991,841-113,992,625 , GRCh37.p13 chr2: 114,749,418-114,750,202 LINC01191
    nsv6686001copy number variation1nstd229human GRCh38 chr2: 113,992,377-113,999,325 , GRCh37.p13 chr2: 114,749,954-114,756,902 LINC01191
    nsv6636454copy number variation1nstd102humanUncertain significance GRCh37 chr2: 114,421,344-115,872,943 , GRCh38.p12 chr2: 113,663,767-115,115,366 MIR4782, LOC105373575, 13 more genes
    nsv6553311inversion1nstd223human GRCh38 chr2: 113,382,126-121,687,299 , GRCh37.p13 chr2: 114,139,703-122,444,875 RPSAP23, CCDC93, 98 more genes
    nsv6543841inversion1nstd223human GRCh38 chr2: 114,002,866-114,004,585 , GRCh37.p13 chr2: 114,760,443-114,762,162 LINC01191
    nsv6354739copy number variation1nstd223human GRCh38 chr2: 114,013,249-114,013,611 , GRCh37.p13 chr2: 114,770,826-114,771,188 LINC01191
    nsv6350421copy number variation1nstd223human GRCh38 chr2: 113,993,707-113,994,103 , GRCh37.p13 chr2: 114,751,284-114,751,680 LINC01191
    nsv6338701copy number variation1nstd223human GRCh38 chr2: 113,994,932-113,995,831 , GRCh37.p13 chr2: 114,752,509-114,753,408 LINC01191
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
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