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Items: 1 to 20 of 242

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7143533copy number variation1nstd232human GRCh37.p13 chr19: 49,964,361-49,964,612 , GRCh38.p12 chr19: 49,461,104-49,461,355 ALDH16A1
    nsv7075539inversion1nstd229human GRCh38 chr19: 48,377,786-50,073,353 , GRCh37.p13 chr19: 48,881,043-50,576,610 SNRNP70, PTOV1, 126 more genes
    nsv7075255inversion1nstd229human GRCh38 chr19: 49,270,356-54,089,823 , GRCh37.p13 chr19: 49,773,613-54,528,887 FPR2, SNAR-A11, 344 more genes
    nsv7075147inversion1nstd229human GRCh38 chr19: 49,467,064-49,473,885 , GRCh37.p13 chr19: 49,970,321-49,977,142 ALDH16A1, FLT3LG
    nsv7074377inversion1nstd229human GRCh38 chr19: 41,965,396-49,981,454 , GRCh37.p13 chr19: 42,514,712-50,484,711 IGFL1, SYMPK, 400 more genes
    nsv7064020inversion1nstd229human GRCh38 chr19: 48,004,601-50,148,757 , GRCh37.p13 chr19: 48,507,858-50,652,014 TEAD2, LHB, 155 more genes
    nsv6595834inversion1nstd223human GRCh38 chr19: 48,004,600-50,148,749 , GRCh37.p13 chr19: 48,507,857-50,652,006 KDELR1, VRK3, 155 more genes
    nsv6534117copy number variation1nstd223human GRCh38 chr19: 49,455,072-49,455,460 , GRCh37.p13 chr19: 49,958,329-49,958,717 ALDH16A1
    nsv6313906copy number variation1nstd102humanLikely pathogenic GRCh37 chr19: 49,911,081-53,127,438 , GRCh38.p12 chr19: 49,407,824-52,624,185 AP2A1, KLK3, 212 more genes
    nsv6310544copy number variation1nstd102humanUncertain significance GRCh37 chr19: 49,519,325-50,366,015 , GRCh38.p12 chr19: 49,016,068-49,862,758 CGB5, MED25, 76 more genes
    nsv6282795copy number variation1nstd214human GRCh38 chr19: 49,461,052-49,461,123 , GRCh37.p13 chr19: 49,964,309-49,964,380 ALDH16A1
    nsv6225788copy number variation1nstd214human GRCh38 chr19: 49,461,163-49,461,234 , GRCh37.p13 chr19: 49,964,420-49,964,491 ALDH16A1
    nsv6223929copy number variation1nstd214human GRCh38 chr19: 49,462,851-49,462,922 , GRCh37.p13 chr19: 49,966,108-49,966,179 ALDH16A1
    nsv6221554copy number variation1nstd214human GRCh38 chr19: 49,461,406-49,461,550 , GRCh37.p13 chr19: 49,964,663-49,964,807 ALDH16A1
    nsv6220133copy number variation1nstd214human GRCh38 chr19: 49,461,370-49,461,550 , GRCh37.p13 chr19: 49,964,627-49,964,807 ALDH16A1
    nsv6216058copy number variation1nstd214human GRCh38 chr19: 49,461,478-49,461,550 , GRCh37.p13 chr19: 49,964,735-49,964,807 ALDH16A1
    nsv6215429copy number variation1nstd214human GRCh38 chr19: 49,463,631-49,463,704 , GRCh37.p13 chr19: 49,966,888-49,966,961 ALDH16A1
    nsv6215426copy number variation1nstd214human GRCh38 chr19: 49,461,162-49,461,327 , GRCh37.p13 chr19: 49,964,419-49,964,584 ALDH16A1
    nsv6212425copy number variation1nstd214human GRCh38 chr19: 49,461,441-49,461,550 , GRCh37.p13 chr19: 49,964,698-49,964,807 ALDH16A1
    nsv6211680copy number variation1nstd214human GRCh38 chr19: 49,462,878-49,463,019 , GRCh37.p13 chr19: 49,966,135-49,966,276 ALDH16A1
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