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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7041761inversion1nstd229human GRCh38 chr2: 161,208,254-165,696,625 , GRCh37.p13 chr2: 162,064,765-166,553,135 SCN3A, LOC101929532, 45 more genes
    nsv7039552inversion1nstd229human GRCh38 chr2: 161,275,467-165,696,611 , GRCh37.p13 chr2: 162,131,978-166,553,121 LOC105373722, EIF3EP3, 42 more genes
    nsv6697136copy number variation1nstd229human GRCh38 chr2: 163,734,850-163,824,879 , GRCh37.p13 chr2: 164,591,360-164,681,389 FIGN
    nsv6695250copy number variation1nstd229human GRCh38 chr2: 163,676,401-163,681,300 , GRCh37.p13 chr2: 164,532,911-164,537,810 FIGN
    nsv6694574copy number variation1nstd229human GRCh38 chr2: 163,714,668-163,723,649 , GRCh37.p13 chr2: 164,571,178-164,580,159 FIGN
    nsv6691515copy number variation1nstd229human GRCh38 chr2: 163,582,449-163,609,129 , GRCh37.p13 chr2: 164,438,959-164,465,639 FIGN
    nsv6689516copy number variation1nstd229human GRCh38 chr2: 163,724,318-163,724,484 , GRCh37.p13 chr2: 164,580,828-164,580,994 FIGN
    nsv6689291copy number variation1nstd229human GRCh38 chr2: 163,686,801-163,690,300 , GRCh37.p13 chr2: 164,543,311-164,546,810 FIGN
    nsv6688521copy number variation1nstd229human GRCh38 chr2: 163,686,751-163,690,351 , GRCh37.p13 chr2: 164,543,261-164,546,861 FIGN
    nsv6683321copy number variation1nstd229human GRCh38 chr2: 163,713,845-163,714,012 , GRCh37.p13 chr2: 164,570,355-164,570,522 FIGN
    nsv6680013copy number variation1nstd229human GRCh38 chr2: 163,616,290-163,618,911 , GRCh37.p13 chr2: 164,472,800-164,475,421 FIGN
    nsv6549853inversion1nstd223human GRCh38 chr2: 163,663,385-163,663,723 , GRCh37.p13 chr2: 164,519,895-164,520,233 FIGN
    nsv6535934inversion1nstd223human GRCh38 chr2: 163,636,347-163,636,954 , GRCh37.p13 chr2: 164,492,857-164,493,464 FIGN
    nsv6351195copy number variation1nstd223human GRCh38 chr2: 163,613,869-163,614,420 , GRCh37.p13 chr2: 164,470,379-164,470,930 FIGN
    nsv6348598copy number variation1nstd223human GRCh38 chr2: 163,697,345-163,697,832 , GRCh37.p13 chr2: 164,553,855-164,554,342 FIGN
    nsv6344281copy number variation1nstd223human GRCh38 chr2: 163,714,668-163,723,646 , GRCh37.p13 chr2: 164,571,178-164,580,156 FIGN
    nsv6342953copy number variation1nstd223human GRCh38 chr2: 163,718,306-163,718,767 , GRCh37.p13 chr2: 164,574,816-164,575,277 FIGN
    nsv6342579copy number variation1nstd223human GRCh38 chr2: 163,623,201-163,624,300 , GRCh37.p13 chr2: 164,479,711-164,480,810 FIGN
    nsv6340826copy number variation1nstd223human GRCh38 chr2: 163,694,759-163,695,285 , GRCh37.p13 chr2: 164,551,269-164,551,795 FIGN
    nsv6336895copy number variation1nstd223human GRCh38 chr2: 163,639,061-163,639,629 , GRCh37.p13 chr2: 164,495,571-164,496,139 FIGN
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