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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6307198copy number variation1nstd186human GRCh37 chr19: 197,700-206,000 , GRCh38.p12 chr19: 197,700-206,000 LINC01002, LOC101928344
    nsv6144667copy number variation1nstd206human GRCh38 chr19: 197,700-206,000 , GRCh37.p13 chr19: 197,700-206,000 LOC101928344, LINC01002
    nsv6133692copy number variation1nstd213human GRCh37 chr19: 180,000-2,200,001 , GRCh38.p12 chr19: 180,000-2,200,002 ATP5F1D, AZU1, 113 more genes
    nsv6116250copy number variation1nstd186human GRCh37 chr19: 88,000-200,000 , GRCh38.p12 chr19: 88,000-200,000 OR4G3P, OR4G1P, 6 more genes
    nsv6113405copy number variation1nstd186human GRCh37 chr19: 196,000-206,000 , GRCh38.p12 chr19: 196,000-206,000 LINC01002, CICP19, 1 more genes
    nsv6112532insertion1nstd212human GRCh38 chr19: 198,450-198,450 , GRCh37.p13 chr19: 198,450-198,450 LINC01002
    nsv6111837insertion1nstd212human GRCh38 chr19: 198,120-198,120 , GRCh37.p13 chr19: 198,120-198,120 LINC01002
    nsv6109711insertion1nstd212human GRCh38 chr19: 198,852-198,852 , GRCh37.p13 chr19: 198,852-198,852 LINC01002
    nsv6109307insertion1nstd212human GRCh38 chr19: 199,041-199,041 , GRCh37.p13 chr19: 199,041-199,041 LINC01002
    nsv6102229insertion1nstd212human GRCh38 chr19: 198,718-198,718 , GRCh37.p13 chr19: 198,718-198,718 LINC01002
    nsv6101169insertion1nstd212human GRCh38 chr19: 199,107-199,107 , GRCh37.p13 chr19: 199,107-199,107 LINC01002
    nsv6040194copy number variation1nstd212human GRCh38 chr19: 199,525-199,644 , GRCh37.p13 chr19: 199,525-199,644 LINC01002
    nsv6038418copy number variation1nstd212human GRCh38 chr19: 198,943-199,037 , GRCh37.p13 chr19: 198,943-199,037 LINC01002
    nsv6032694copy number variation1nstd212human GRCh38 chr19: 198,855-198,950 , GRCh37.p13 chr19: 198,855-198,950 LINC01002
    nsv6032538copy number variation1nstd212human GRCh38 chr19: 198,640-198,737 , GRCh37.p13 chr19: 198,640-198,737 LINC01002
    nsv6031134copy number variation1nstd212human GRCh38 chr19: 199,585-199,681 , GRCh37.p13 chr19: 199,585-199,681 LINC01002
    nsv5602740copy number variation1nstd207human GRCh38 chr19: 198,343-198,633 , GRCh37.p13 chr19: 198,343-198,633 LINC01002
    nsv5596845copy number variation1nstd207human GRCh38 chr19: 201,677-204,841 , GRCh37.p13 chr19: 201,677-204,841 LINC01002, LOC101928344
    nsv5594139copy number variation1nstd207human GRCh38 chr19: 194,513-205,777 , GRCh37.p13 chr19: 194,513-205,777 LINC01002, CICP19, 1 more genes
    nsv5591443copy number variation1nstd207human GRCh38 chr19: 198,717-198,813 , GRCh37.p13 chr19: 198,717-198,813 LINC01002
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