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Items: 1 to 20 of 222

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099199copy number variation1nstd231human GRCh38.p12 chr1: 47,175,123-48,269,119 , GRCh37 chr1: 47,640,795-48,734,791 FOXE3, FOXD2, 17 more genes
    nsv7052650inversion1nstd229human GRCh38 chr1: 47,584,744-54,395,558 , GRCh37.p13 chr1: 48,050,416-54,861,231 ANAPC10P1, SPATA6, 137 more genes
    nsv7050558inversion1nstd229human GRCh38 chr1: 48,116,108-48,813,202 , GRCh37.p13 chr1: 48,581,780-49,278,874 RPL21P25, SKINT1L, 9 more genes
    nsv6651035copy number variation1nstd229human GRCh38 chr1: 48,244,280-48,257,509 , GRCh37.p13 chr1: 48,709,952-48,723,181 SPATA6, SLC5A9
    nsv6650959copy number variation1nstd229human GRCh38 chr1: 48,237,101-48,245,900 , GRCh37.p13 chr1: 48,702,773-48,711,572 SLC5A9
    nsv6650958copy number variation1nstd229human GRCh38 chr1: 48,229,624-48,234,000 , GRCh37.p13 chr1: 48,695,296-48,699,672 SLC5A9
    nsv6650956copy number variation1nstd229human GRCh38 chr1: 48,177,335-48,224,339 , GRCh37.p13 chr1: 48,643,007-48,690,011 SLC5A9, LINC02794, 1 more genes
    nsv6650817copy number variation1nstd229human GRCh38 chr1: 48,224,926-48,230,963 , GRCh37.p13 chr1: 48,690,598-48,696,635 SLC5A9
    nsv6650816copy number variation1nstd229human GRCh38 chr1: 48,219,215-48,228,927 , GRCh37.p13 chr1: 48,684,887-48,694,599 SLC5A9
    nsv6636718copy number variation1nstd102humanUncertain significance GRCh37 chr1: 48,634,963-48,702,484 , GRCh38.p12 chr1: 48,169,291-48,236,812 SLC5A9, LINC02794, 1 more genes
    nsv6626455copy number variation1nstd224human GRCh37 chr1: 48,672,401-48,802,740 , GRCh38.p12 chr1: 48,206,729-48,337,068 SPATA6, SLC5A9, 1 more genes
    nsv6539466inversion1nstd223human GRCh38 chr1: 48,225,826-48,227,367 , GRCh37.p13 chr1: 48,691,498-48,693,039 SLC5A9
    nsv6326236copy number variation1nstd223human GRCh38 chr1: 48,219,215-48,228,927 , GRCh37.p13 chr1: 48,684,887-48,694,599 SLC5A9
    nsv6325938copy number variation1nstd223human GRCh38 chr1: 48,177,335-48,224,333 , GRCh37.p13 chr1: 48,643,007-48,690,005 LINC02794, SKINT1L, 1 more genes
    nsv6320273copy number variation1nstd223human GRCh38 chr1: 48,197,628-48,329,739 , GRCh37.p13 chr1: 48,663,300-48,795,411 SPATA6, SLC5A9, 1 more genes
    nsv6320203copy number variation1nstd223human GRCh38 chr1: 47,992,330-48,762,028 , GRCh37.p13 chr1: 48,458,002-49,227,700 RNU6-723P, RNU4-61P, 11 more genes
    nsv6290448copy number variation1nstd102humanUncertain significance GRCh37 chr1: 48,634,962-48,697,751 , GRCh38.p12 chr1: 48,169,290-48,232,079 SLC5A9, LINC02794, 1 more genes
    nsv6158621copy number variation1nstd214human GRCh38 chr1: 48,227,282-48,227,373 , GRCh37.p13 chr1: 48,692,954-48,693,045 SLC5A9
    nsv6047612insertion1nstd212human GRCh38 chr1: 48,244,736-48,244,736 , GRCh37.p13 chr1: 48,710,408-48,710,408 SLC5A9
    nsv5984353copy number variation1nstd212human GRCh38 chr1: 48,227,282-48,227,378 , GRCh37.p13 chr1: 48,692,954-48,693,050 SLC5A9
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