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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3878885copy number variation1nstd102humanBenign GRCh37 chr2: 77,643,760-77,659,859 , GRCh38.p12 chr2: 77,416,634-77,432,733 LRRTM4
    nsv3871736copy number variation1nstd102humanBenign GRCh37 chr2: 77,100,771-77,101,651 , GRCh38.p12 chr2: 76,873,645-76,874,525 LRRTM4
    nsv3878171copy number variation1nstd102humanBenign GRCh37 chr2: 77,395,150-77,445,569 , GRCh38.p12 chr2: 77,168,024-77,218,443 LRRTM4
    nsv508095sequence alteration1nstd49human NCBI35 chr2: 77,602,325-77,608,325 , GRCh37.p13 chr2: 77,690,670-77,696,670 , GRCh38.p12 chr2: 77,463,544-77,469,544 LRRTM4
    nsv6692251copy number variation1nstd229human GRCh38 chr2: 77,483,115-77,663,148 , GRCh37.p13 chr2: 77,710,241-77,890,274 LRRTM4
    nsv6687618copy number variation1nstd229human GRCh38 chr2: 77,036,501-77,186,800 , GRCh37.p13 chr2: 77,263,627-77,413,926 LRRTM4
    nsv6682735copy number variation1nstd229human GRCh38 chr2: 77,432,401-77,526,100 , GRCh37.p13 chr2: 77,659,527-77,753,226 LRRTM4
    nsv6693372copy number variation1nstd229human GRCh38 chr2: 77,349,600-77,443,261 , GRCh37.p13 chr2: 77,576,726-77,670,387 LRRTM4
    nsv6680211copy number variation1nstd229human GRCh38 chr2: 77,426,821-77,463,742 , GRCh37.p13 chr2: 77,653,947-77,690,868 LRRTM4
    nsv6689537copy number variation1nstd229human GRCh38 chr2: 77,208,289-77,241,142 , GRCh37.p13 chr2: 77,435,415-77,468,268 LRRTM4
    nsv6690296copy number variation1nstd229human GRCh38 chr2: 76,950,901-76,980,500 , GRCh37.p13 chr2: 77,178,027-77,207,626 LRRTM4
    nsv6691278copy number variation1nstd229human GRCh38 chr2: 77,369,671-77,395,007 , GRCh37.p13 chr2: 77,596,797-77,622,133 LRRTM4
    nsv6687418copy number variation1nstd229human GRCh38 chr2: 77,065,947-77,086,607 , GRCh37.p13 chr2: 77,293,073-77,313,733 LRRTM4
    nsv6682280copy number variation1nstd229human GRCh38 chr2: 77,177,784-77,198,105 , GRCh37.p13 chr2: 77,404,910-77,425,231 LRRTM4
    nsv6697689copy number variation1nstd229human GRCh38 chr2: 77,083,800-77,103,212 , GRCh37.p13 chr2: 77,310,926-77,330,338 LRRTM4
    nsv6697013copy number variation1nstd229human GRCh38 chr2: 77,416,249-77,433,581 , GRCh37.p13 chr2: 77,643,375-77,660,707 LRRTM4
    nsv6696737copy number variation1nstd229human GRCh38 chr2: 77,129,401-77,141,500 , GRCh37.p13 chr2: 77,356,527-77,368,626 LRRTM4
    nsv6683896copy number variation1nstd229human GRCh38 chr2: 77,391,742-77,403,272 , GRCh37.p13 chr2: 77,618,868-77,630,398 LRRTM4
    nsv6678537copy number variation1nstd229human GRCh38 chr2: 77,130,292-77,141,477 , GRCh37.p13 chr2: 77,357,418-77,368,603 LRRTM4
    nsv6683013copy number variation1nstd229human GRCh38 chr2: 77,449,494-77,460,378 , GRCh37.p13 chr2: 77,676,620-77,687,504 LRRTM4
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