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Items: 1 to 20 of 929

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978376insertion1nstd209human GRCh38 chr12: 13,692,760-13,692,760 , GRCh37.p13 chr12: 13,845,694-13,845,694 GRIN2B
    nsv5970742insertion1nstd209human GRCh38 chr12: 13,954,811-13,954,811 , GRCh37.p13 chr12: 14,107,745-14,107,745 GRIN2B
    nsv5925880copy number variation1nstd209human GRCh38 chr12: 13,934,663-13,934,854 , GRCh37.p13 chr12: 14,087,597-14,087,788 GRIN2B
    nsv5922060copy number variation1nstd209human GRCh38 chr12: 13,572,971-13,573,618 , GRCh37.p13 chr12: 13,725,905-13,726,552 GRIN2B
    nsv5921370copy number variation1nstd209human GRCh38 chr12: 13,688,128-13,688,269 , GRCh37.p13 chr12: 13,841,062-13,841,203 GRIN2B
    nsv5919557copy number variation1nstd209human GRCh38 chr12: 13,899,389-13,899,880 , GRCh37.p13 chr12: 14,052,323-14,052,814 GRIN2B
    nsv5908245copy number variation1nstd209human GRCh38 chr12: 13,788,675-13,788,771 , GRCh37.p13 chr12: 13,941,609-13,941,705 GRIN2B
    nsv5865330copy number variation1nstd209human GRCh38 chr12: 13,817,486-13,820,085 , GRCh37.p13 chr12: 13,970,420-13,973,019 GRIN2B
    nsv5723457mobile element insertion1nstd211human GRCh38 chr12: 13,705,194-13,705,194 , GRCh37.p13 chr12: 13,858,128-13,858,128 GRIN2B
    nsv5720000mobile element insertion1nstd211human GRCh38 chr12: 13,619,601-13,619,601 , GRCh37.p13 chr12: 13,772,535-13,772,535 LOC105369668, GRIN2B
    nsv5718414mobile element insertion2nstd211human GRCh38 chr12: 13,728,961-13,728,961 , GRCh37.p13 chr12: 13,881,895-13,881,895 GRIN2B
    nsv5708262mobile element insertion1nstd211human GRCh38 chr12: 13,825,494-13,825,494 , GRCh37.p13 chr12: 13,978,428-13,978,428 GRIN2B, LOC105369667
    nsv5695951mobile element insertion2nstd211human GRCh38 chr12: 13,837,652-13,837,652 , GRCh37.p13 chr12: 13,990,586-13,990,586 GRIN2B, LOC105369667
    nsv5653843insertion1nstd207human GRCh38 chr12: 13,607,270-13,607,270 , GRCh37.p13 chr12: 13,760,204-13,760,204 LOC105369668, GRIN2B
    nsv5603491copy number variation1nstd207human GRCh38 chr12: 13,934,663-13,934,854 , GRCh37.p13 chr12: 14,087,597-14,087,788 GRIN2B
    nsv5601772copy number variation1nstd207human GRCh38 chr12: 13,572,971-13,573,618 , GRCh37.p13 chr12: 13,725,905-13,726,552 GRIN2B
    nsv5591553copy number variation1nstd207human GRCh38 chr12: 13,607,320-13,607,376 , GRCh37.p13 chr12: 13,760,254-13,760,310 LOC105369668, GRIN2B
    nsv5589774copy number variation1nstd207human GRCh38 chr12: 13,712,460-13,721,440 , GRCh37.p13 chr12: 13,865,394-13,874,374 GRIN2B
    nsv5586506copy number variation1nstd207human GRCh38 chr12: 13,899,392-13,899,883 , GRCh37.p13 chr12: 14,052,326-14,052,817 GRIN2B
    nsv5585292copy number variation1nstd207human GRCh38 chr12: 13,788,675-13,788,771 , GRCh37.p13 chr12: 13,941,609-13,941,705 GRIN2B
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