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Items: 1 to 20 of 197

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5973866insertion1nstd209human GRCh38 chr12: 96,932,463-96,932,463 , GRCh37.p13 chr12: 97,326,241-97,326,241 NEDD1
    nsv5708400mobile element insertion1nstd211human GRCh38 chr12: 96,905,982-96,905,982 , GRCh37.p13 chr12: 97,299,760-97,299,760 NEDD1
    nsv5707303mobile element insertion2nstd211human GRCh38 chr12: 96,953,550-96,953,550 , GRCh37.p13 chr12: 97,347,328-97,347,328 NEDD1
    nsv5701745mobile element insertion1nstd211human GRCh38 chr12: 96,929,624-96,929,624 , GRCh37.p13 chr12: 97,323,402-97,323,402 NEDD1
    nsv5417160mobile element insertion1nstd206human GRCh38 chr12: 96,953,550-96,953,601 , GRCh37.p13 chr12: 97,347,328-97,347,379 NEDD1
    nsv5416164mobile element insertion1nstd206human GRCh38 chr12: 96,905,982-96,906,033 , GRCh37.p13 chr12: 97,299,760-97,299,811 NEDD1
    nsv5272353copy number variation1nstd204human GRCh38.p13 chr12: 96,949,801-96,960,100 , GRCh37.p13 chr12: 97,343,579-97,353,878 NEDD1
    nsv5262278copy number variation1nstd204human GRCh38.p13 chr12: 96,949,201-96,954,400 , GRCh37.p13 chr12: 97,342,979-97,348,178 NEDD1
    nsv5189027mobile element insertion1nstd203human GRCh38 chr12: 96,952,211-96,952,229 , GRCh37.p13 chr12: 97,345,989-97,346,007 NEDD1
    nsv5136281mobile element insertion1nstd203human GRCh38 chr12: 96,905,968-96,905,979 , GRCh37.p13 chr12: 97,299,746-97,299,757 NEDD1
    nsv5135870mobile element insertion1nstd203human GRCh38 chr12: 96,943,553-96,943,572 , GRCh37.p13 chr12: 97,337,331-97,337,350 NEDD1
    nsv5132702mobile element insertion1nstd203human GRCh38 chr12: 96,934,555-96,934,564 , GRCh37.p13 chr12: 97,328,333-97,328,342 NEDD1
    nsv5129884mobile element insertion1nstd203human GRCh38 chr12: 96,953,536-96,953,550 , GRCh37.p13 chr12: 97,347,314-97,347,328 NEDD1
    nsv5123731mobile element insertion1nstd203human GRCh38 chr12: 96,932,463-96,932,463 , GRCh37.p13 chr12: 97,326,241-97,326,241 NEDD1
    nsv5037136inversion1nstd200human GRCh38 chr12: 69,787,024-109,882,221 , GRCh37.p13 chr12: 70,180,804-110,320,026 , RPL23AP68, 540 more genes
    nsv4886161inversion1nstd200human GRCh37 chr12: 70,180,810-110,320,027 , GRCh38.p12 chr12: 69,787,030-109,882,222 , LOC728739, 540 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4611599copy number variation1nstd183human GRCh37 chr12: 97,311,447-97,313,698 , GRCh38.p12 chr12: 96,917,669-96,919,920 NEDD1
    nsv4611503copy number variation1nstd183human GRCh37 chr12: 97,330,781-97,331,012 , GRCh38.p12 chr12: 96,937,003-96,937,234 NEDD1
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