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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094111copy number variation1nstd102humanPathogenic GRCh37 chr11: 85,339,652-86,666,127 , GRCh38.p12 chr11: 85,628,608-86,955,085 PRSS23, OR7E13P, 30 more genes
    nsv7093948copy number variation1nstd102humanUncertain significance GRCh37 chr11: 85,339,652-85,367,545 , GRCh38.p12 chr11: 85,628,608-85,656,501 CREBZF, TMEM126B, 2 more genes
    nsv7068892inversion1nstd229human GRCh38 chr11: 85,482,651-87,653,297 , GRCh37.p13 chr11: 85,193,695-87,364,189 , RNU6-1292P, 42 more genes
    nsv7062534inversion1nstd229human GRCh38 chr11: 83,132,580-86,771,462 , GRCh37.p13 chr11: 82,843,622-86,482,504 CCDC83, LOC100421303, 44 more genes
    nsv6915767copy number variation1nstd229human GRCh38 chr11: 85,680,704-85,696,695 , GRCh37.p13 chr11: 85,391,748-85,407,738 CCDC89, CREBZF, 1 more genes
    nsv6914106copy number variation1nstd229human GRCh38 chr11: 85,494,651-85,925,994 , GRCh37.p13 chr11: 85,205,695-85,637,037 SYTL2, CREBZF, 7 more genes
    nsv6911289copy number variation1nstd229human GRCh38 chr11: 85,668,727-85,685,428 , GRCh37.p13 chr11: 85,379,771-85,396,471 CCDC89, CREBZF
    nsv6909401copy number variation1nstd229human GRCh38 chr11: 85,666,651-85,669,892 , GRCh37.p13 chr11: 85,377,695-85,380,936 CREBZF
    nsv6905973copy number variation1nstd229human GRCh38 chr11: 85,659,456-85,668,223 , GRCh37.p13 chr11: 85,370,500-85,379,267 CREBZF
    nsv6905543copy number variation1nstd229human GRCh38 chr11: 84,763,504-86,648,143 , GRCh37.p13 chr11: 84,474,547-86,359,185 CCDC83, CCDC81, 25 more genes
    nsv6903585copy number variation1nstd229human GRCh38 chr11: 85,662,791-85,753,611 , GRCh37.p13 chr11: 85,373,835-85,464,654 CREBZF, SYTL2, 1 more genes
    nsv6902729copy number variation1nstd229human GRCh38 chr11: 85,669,807-85,670,653 , GRCh37.p13 chr11: 85,380,851-85,381,697 CREBZF
    nsv6902416copy number variation1nstd229human GRCh38 chr11: 85,286,883-85,726,573 , GRCh37.p13 chr11: 84,997,927-85,437,616 RNU6-1292P, LOC100419092, 7 more genes
    nsv6901239copy number variation1nstd229human GRCh38 chr11: 85,654,490-85,732,964 , GRCh37.p13 chr11: 85,365,534-85,444,007 CCDC89, TMEM126A, 2 more genes
    nsv6900558copy number variation1nstd229human GRCh38 chr11: 85,674,297-85,674,641 , GRCh37.p13 chr11: 85,385,341-85,385,685 CREBZF
    nsv6637847copy number variation1nstd102humanPathogenic GRCh37 chr11: 80,562,738-88,663,067 , GRCh38.p12 chr11: 80,851,695-88,929,899 PRSS23, MTCO3P25, 92 more genes
    nsv6637396copy number variation1nstd102humanPathogenic GRCh37 chr11: 81,478,509-104,667,040 , GRCh38.p12 chr11: 81,767,467-104,796,313 LOC107984375, RN7SL222P, 295 more genes
    nsv6584412inversion1nstd223human GRCh38 chr11: 85,506,446-86,544,042 , GRCh37.p13 chr11: 85,217,490-86,255,084 RNU6-1292P, CCDC81, 22 more genes
    nsv6462238copy number variation1nstd223human GRCh38 chr11: 84,663,295-85,663,452 , GRCh37.p13 chr11: 84,374,338-85,374,496 TMEM126B, TMEM126A, 6 more genes
    nsv6461726copy number variation1nstd223human GRCh38 chr11: 85,667,001-85,670,500 , GRCh37.p13 chr11: 85,378,045-85,381,544 CREBZF
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