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Items: 1 to 20 of 939

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140935copy number variation1nstd232human GRCh37.p13 chr12: 13,941,609-13,941,705 , GRCh38.p12 chr12: 13,788,675-13,788,771 GRIN2B
    nsv7137099copy number variation1nstd102humanPathogenic GRCh37 chr12: 11,463,270-14,019,142 , GRCh38.p12 chr12: 11,310,336-13,866,208 HTR7P1, RPL37AP9, 55 more genes
    nsv7098813copy number variation1nstd102humanPathogenic GRCh37 chr12: 176,047-34,179,852 , GRCh38.p12 chr12: 66,881-34,026,917 TDGP1, RPS4XP14, 680 more genes
    nsv7094208copy number variation1nstd102humanPathogenic GRCh37 chr12: 13,828,659-13,828,813 , GRCh38.p12 chr12: 13,675,725-13,675,879 GRIN2B
    nsv7094135copy number variation1nstd102humanUncertain significance GRCh37 chr12: 13,715,717-14,019,142 , GRCh38.p12 chr12: 13,562,783-13,866,208 RN7SKP162, GRIN2B, 2 more genes
    nsv7075742inversion1nstd229human GRCh38 chr12: 13,625,374-13,625,472 , GRCh37.p13 chr12: 13,778,308-13,778,406 GRIN2B
    nsv7073678inversion1nstd229human GRCh38 chr12: 13,652,146-13,652,424 , GRCh37.p13 chr12: 13,805,080-13,805,358 GRIN2B
    nsv7067745inversion1nstd229human GRCh38 chr12: 13,618,040-13,621,090 , GRCh37.p13 chr12: 13,770,974-13,774,024 GRIN2B, LOC105369668
    nsv7066753inversion1nstd229human GRCh38 chr12: 13,755,934-13,776,554 , GRCh37.p13 chr12: 13,908,868-13,929,488 GRIN2B
    nsv7064011inversion1nstd229human GRCh38 chr12: 11,255,910-17,864,916 , GRCh37.p13 chr12: 11,408,826-18,017,850 MGP, MIR3974, 108 more genes
    nsv7061113inversion1nstd229human GRCh38 chr12: 13,546,488-13,550,435 , GRCh37.p13 chr12: 13,699,422-13,703,369 GRIN2B
    nsv6937919copy number variation1nstd229human GRCh38 chr12: 13,635,220-13,640,946 , GRCh37.p13 chr12: 13,788,154-13,793,880 GRIN2B
    nsv6937837copy number variation1nstd229human GRCh38 chr12: 13,761,924-13,770,237 , GRCh37.p13 chr12: 13,914,858-13,923,171 GRIN2B
    nsv6937489copy number variation1nstd229human GRCh38 chr12: 13,826,971-13,826,995 , GRCh37.p13 chr12: 13,979,905-13,979,929 GRIN2B, LOC105369667
    nsv6936975copy number variation1nstd229human GRCh38 chr12: 13,677,000-13,680,108 , GRCh37.p13 chr12: 13,829,934-13,833,042 GRIN2B
    nsv6936722copy number variation1nstd229human GRCh38 chr12: 13,934,667-13,934,855 , GRCh37.p13 chr12: 14,087,601-14,087,789 GRIN2B
    nsv6935963copy number variation1nstd229human GRCh38 chr12: 13,586,418-13,586,615 , GRCh37.p13 chr12: 13,739,352-13,739,549 LOC105369668, GRIN2B
    nsv6935298copy number variation1nstd229human GRCh38 chr12: 13,907,413-13,921,940 , GRCh37.p13 chr12: 14,060,347-14,074,874 GRIN2B
    nsv6934633copy number variation1nstd229human GRCh38 chr12: 13,557,845-13,558,350 , GRCh37.p13 chr12: 13,710,779-13,711,284 GRIN2B
    nsv6933722copy number variation1nstd229human GRCh38 chr12: 13,708,041-13,747,651 , GRCh37.p13 chr12: 13,860,975-13,900,585 GRIN2B
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