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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5978755inversion1nstd209human GRCh38 chr19: 21,483,880-21,483,948 , GRCh37.p13 chr19: 21,666,682-21,666,750 LINC00664
    nsv5936015copy number variation1nstd209human GRCh38 chr19: 21,494,308-21,498,648 , GRCh37.p13 chr19: 21,677,110-21,681,450 LINC00664
    nsv5931832copy number variation1nstd209human GRCh38 chr19: 21,483,074-21,483,148 , GRCh37.p13 chr19: 21,665,876-21,665,950 LINC00664
    nsv5930276copy number variation1nstd209human GRCh38 chr19: 21,439,885-21,545,621 , GRCh37.p13 chr19: 21,622,687-21,728,423 ZNF429, LINC00664, 2 more genes
    nsv5716813mobile element insertion2nstd211human GRCh38 chr19: 21,495,500-21,495,500 , GRCh37.p13 chr19: 21,678,302-21,678,302 LINC00664
    nsv5702843mobile element insertion1nstd211human GRCh38 chr19: 21,486,344-21,486,344 , GRCh37.p13 chr19: 21,669,146-21,669,146 LINC00664
    nsv5649792insertion1nstd207human GRCh38 chr19: 21,484,239-21,484,239 , GRCh37.p13 chr19: 21,667,041-21,667,041 LINC00664
    nsv5556184mobile element insertion1nstd206human GRCh38 chr19: 21,495,500-21,495,551 , GRCh37.p13 chr19: 21,678,302-21,678,353 LINC00664
    nsv5543848insertion1nstd206human GRCh38 chr19: 21,484,187-21,484,221 , GRCh37.p13 chr19: 21,666,989-21,667,023 LINC00664
    nsv5530094copy number variation1nstd206human GRCh38 chr19: 21,483,074-21,483,151 , GRCh37.p13 chr19: 21,665,876-21,665,953 LINC00664
    nsv5526508copy number variation1nstd206human GRCh38 chr19: 21,489,219-21,492,630 , GRCh37.p13 chr19: 21,672,021-21,675,432 LINC00664
    nsv5514404copy number variation1nstd206human GRCh38 chr19: 21,502,101-21,502,195 , GRCh37.p13 chr19: 21,684,903-21,684,997 LINC00664
    nsv5391587copy number variation1nstd186human GRCh37 chr19: 21,682,826-21,778,292 , GRCh38.p12 chr19: 21,500,024-21,595,490 ZNF429, LINC00664, 3 more genes
    nsv5389832copy number variation1nstd186human GRCh37 chr19: 21,682,753-21,778,292 , GRCh38.p12 chr19: 21,499,951-21,595,490 ZNF429, LINC00664, 3 more genes
    nsv5368928translocation1nstd200human GRCh38 chr19: 21,503,685-21,503,685 , GRCh38 chr5: 129,886,524-129,886,524 , GRCh37.p13 chr19: 21,686,487-21,686,487 , GRCh37.p13 chr5: 129,222,217-129,222,217 ZNF429, LINC00664, 1 more genes
    nsv5339072translocation1nstd200human GRCh37 chr5: 129,222,217-129,222,217 , GRCh37 chr19: 21,686,487-21,686,487 , GRCh38.p12 chr19: 21,503,685-21,503,685 , GRCh38.p12 chr5: 129,886,524-129,886,524 ZNF429, LINC00664, 1 more genes
    nsv5329381copy number variation1nstd204human GRCh38.p13 chr19: 21,499,413-21,596,037 , GRCh37.p13 chr19: 21,682,215-21,778,839 LINC00664, BNIP3P26, 3 more genes
    nsv5324992translocation1nstd204human GRCh38.p13 chr19: 21,503,685-21,503,685 , GRCh37.p13 chr19: 21,686,487-21,686,487 , GRCh37.p13 chr5: 129,222,217-129,222,217 , GRCh38.p13 chr5: 129,886,524-129,886,524 ZNF429, LINC00664, 1 more genes
    nsv5199049mobile element insertion1nstd203human GRCh38 chr19: 21,495,499-21,495,499 , GRCh37.p13 chr19: 21,678,301-21,678,301 LINC00664
    nsv5189453mobile element insertion1nstd203human GRCh38 chr19: 21,495,497-21,495,497 , GRCh37.p13 chr19: 21,678,299-21,678,299 LINC00664
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