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Items: 1 to 20 of 653

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5976978insertion1nstd209human GRCh38 chr18: 9,152,948-9,152,948 , GRCh37.p13 chr18: 9,152,946-9,152,946 ANKRD12
    nsv5968594insertion1nstd209human GRCh38 chr18: 9,157,550-9,157,550 , GRCh37.p13 chr18: 9,157,548-9,157,548 ANKRD12
    nsv5943835copy number variation1nstd209human GRCh38 chr18: 8,888,335-9,169,886 , GRCh37.p13 chr18: 8,888,333-9,169,884 NDUFV2, ANKRD12, 2 more genes
    nsv5937886copy number variation1nstd209human GRCh38 chr18: 9,137,433-9,137,551 , GRCh37.p13 chr18: 9,137,431-9,137,549 ANKRD12
    nsv5937029copy number variation1nstd209human GRCh38 chr18: 9,284,981-9,286,147 , GRCh37.p13 chr18: 9,284,979-9,286,145 ANKRD12
    nsv5935007copy number variation1nstd209human GRCh38 chr18: 9,225,120-9,225,454 , GRCh37.p13 chr18: 9,225,118-9,225,452 ANKRD12
    nsv5930806copy number variation1nstd209human GRCh38 chr18: 9,277,706-9,277,817 , GRCh37.p13 chr18: 9,277,704-9,277,815 , ANKRD12
    nsv5929807copy number variation1nstd209human GRCh38 chr18: 9,225,848-9,225,979 , GRCh37.p13 chr18: 9,225,846-9,225,977 ANKRD12
    nsv5719104mobile element insertion2nstd211human GRCh38 chr18: 9,210,431-9,210,431 , GRCh37.p13 chr18: 9,210,429-9,210,429 ANKRD12
    nsv5711443mobile element insertion1nstd211human GRCh38 chr18: 9,149,790-9,149,790 , GRCh37.p13 chr18: 9,149,788-9,149,788 ANKRD12
    nsv5706943mobile element insertion1nstd211human GRCh38 chr18: 9,175,551-9,175,551 , GRCh37.p13 chr18: 9,175,549-9,175,549 ANKRD12
    nsv5703740mobile element insertion1nstd211human GRCh38 chr18: 9,237,696-9,237,696 , GRCh37.p13 chr18: 9,237,694-9,237,694 ANKRD12
    nsv5695270mobile element insertion1nstd211human GRCh38 chr18: 9,169,044-9,169,044 , GRCh37.p13 chr18: 9,169,042-9,169,042 ANKRD12
    nsv5695062mobile element insertion2nstd211human GRCh38 chr18: 9,152,961-9,152,961 , GRCh37.p13 chr18: 9,152,959-9,152,959 ANKRD12
    nsv5672896copy number variation1nstd102humanPathogenic GRCh37 chr18: 2,656,075-13,885,536 , GRCh38.p12 chr18: 2,656,076-13,885,537 RN7SL862P, LOC105371972, 181 more genes
    nsv5657478insertion1nstd207human GRCh38 chr18: 9,196,122-9,196,122 , GRCh37.p13 chr18: 9,196,120-9,196,120 ANKRD12
    nsv5644924insertion1nstd207human GRCh38 chr18: 9,157,550-9,157,550 , GRCh37.p13 chr18: 9,157,548-9,157,548 ANKRD12
    nsv5593652copy number variation1nstd207human GRCh38 chr18: 9,284,981-9,286,147 , GRCh37.p13 chr18: 9,284,979-9,286,145 ANKRD12
    nsv5593285copy number variation1nstd207human GRCh38 chr18: 9,225,120-9,225,454 , GRCh37.p13 chr18: 9,225,118-9,225,452 ANKRD12
    nsv5587596copy number variation1nstd207human GRCh38 chr18: 9,277,706-9,277,817 , GRCh37.p13 chr18: 9,277,704-9,277,815 , ANKRD12
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