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Items: 1 to 20 of 419

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5899433copy number variation1nstd209human GRCh38 chr2: 154,843,287-154,848,442 , GRCh37.p13 chr2: 155,699,799-155,704,954 KCNJ3
    nsv5831671copy number variation1nstd209human GRCh38 chr2: 154,843,271-154,848,553 , GRCh37.p13 chr2: 155,699,783-155,705,065 KCNJ3
    nsv5691366mobile element insertion2nstd211human GRCh38 chr2: 154,731,648-154,731,648 , GRCh37.p13 chr2: 155,588,160-155,588,160 KCNJ3
    nsv5689720mobile element insertion2nstd211human GRCh38 chr2: 154,843,641-154,843,641 , GRCh37.p13 chr2: 155,700,153-155,700,153 KCNJ3
    nsv5685682mobile element insertion2nstd211human GRCh38 chr2: 154,722,187-154,722,187 , GRCh37.p13 chr2: 155,578,699-155,578,699 KCNJ3
    nsv5560580sequence alteration1nstd206human GRCh38 chr2: 151,447,581-231,256,535 , GRCh37.p13 chr2: 152,304,095-232,121,248 , ATIC, 1163 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5452828copy number variation1nstd206human GRCh38 chr2: 154,843,291-154,848,443 , GRCh37.p13 chr2: 155,699,803-155,704,955 KCNJ3
    nsv5450895copy number variation1nstd206human GRCh38 chr2: 141,459,078-156,842,302 , GRCh37.p13 chr2: 142,216,647-157,698,814 , LOC105373696, 163 more genes
    nsv5448752copy number variation1nstd206human GRCh38 chr2: 154,810,554-154,810,922 , GRCh37.p13 chr2: 155,667,066-155,667,434 KCNJ3
    nsv5434730copy number variation1nstd206human GRCh38 chr2: 148,693,148-164,933,481 , GRCh37.p13 chr2: 149,450,717-165,789,991 , RBM43, 205 more genes
    nsv5410343mobile element insertion1nstd206human GRCh38 chr2: 154,722,187-154,722,238 , GRCh37.p13 chr2: 155,578,699-155,578,750 KCNJ3
    nsv5404554mobile element insertion1nstd206human GRCh38 chr2: 154,731,648-154,731,699 , GRCh37.p13 chr2: 155,588,160-155,588,211 KCNJ3
    nsv5397325mobile element insertion1nstd206human GRCh38 chr2: 154,843,641-154,843,692 , GRCh37.p13 chr2: 155,700,153-155,700,204 KCNJ3
    nsv5366524translocation1nstd200human GRCh38 chr2: 154,748,101-154,748,101 , GRCh38 chr2: 154,749,866-154,749,866 , GRCh37.p13 chr2: 155,604,613-155,604,613 , GRCh37.p13 chr2: 155,606,378-155,606,378 KCNJ3
    nsv5327227inversion1nstd204human GRCh37.p13 chr2: 151,300,232-168,612,803 , GRCh38.p13 chr2: 150,443,718-167,756,293 , RND3, 198 more genes
    nsv5298334copy number variation1nstd204human GRCh38.p13 chr2: 154,844,106-154,847,677 , GRCh37.p13 chr2: 155,700,618-155,704,189 KCNJ3
    nsv5293381copy number variation1nstd204human GRCh38.p13 chr2: 154,835,432-154,835,540 , GRCh37.p13 chr2: 155,691,944-155,692,052 KCNJ3
    nsv5207069copy number variation1nstd204human GRCh38.p13 chr2: 154,844,098-154,847,676 , GRCh37.p13 chr2: 155,700,610-155,704,188 KCNJ3
    nsv5203487copy number variation1nstd204human GRCh38.p13 chr2: 154,844,101-154,847,600 , GRCh37.p13 chr2: 155,700,613-155,704,112 KCNJ3
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