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Items: 1 to 20 of 251

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7049391inversion1nstd229human GRCh38 chr3: 156,782,836-156,782,850 , GRCh37.p13 chr3: 156,500,625-156,500,639 LINC00886
    nsv7047569inversion1nstd229human GRCh38 chr3: 152,490,812-161,531,961 , GRCh37.p13 chr3: 152,208,601-161,249,749 RPS2P19, LOC112268450, 128 more genes
    nsv7042660inversion1nstd229human GRCh38 chr3: 156,770,956-156,771,153 , GRCh37.p13 chr3: 156,488,745-156,488,942 LINC00886
    nsv7042233inversion1nstd229human GRCh38 chr3: 156,741,449-156,823,649 , GRCh37.p13 chr3: 156,459,238-156,541,438 PA2G4P4, LINC00886
    nsv6737716copy number variation1nstd229human GRCh38 chr3: 156,762,601-156,773,200 , GRCh37.p13 chr3: 156,480,390-156,490,989 LINC00886
    nsv6737606copy number variation1nstd229human GRCh38 chr3: 156,795,338-156,803,367 , GRCh37.p13 chr3: 156,513,127-156,521,156 LINC00886
    nsv6737027copy number variation1nstd229human GRCh38 chr3: 156,808,287-156,815,394 , GRCh37.p13 chr3: 156,526,076-156,533,183 PA2G4P4, LINC00886
    nsv6734371copy number variation1nstd229human GRCh38 chr3: 156,578,264-157,290,961 , GRCh37.p13 chr3: 156,296,053-157,008,750 PA2G4P4, METTL15P1, 17 more genes
    nsv6728130copy number variation1nstd229human GRCh38 chr3: 156,804,750-156,807,856 , GRCh37.p13 chr3: 156,522,539-156,525,645 PA2G4P4, LINC00886
    nsv6728055copy number variation1nstd229human GRCh38 chr3: 156,788,033-156,788,144 , GRCh37.p13 chr3: 156,505,822-156,505,933 LINC00886
    nsv6727564copy number variation1nstd229human GRCh38 chr3: 156,645,897-156,749,368 , GRCh37.p13 chr3: 156,363,686-156,467,157 TIPARP-AS1, LINC00886, 2 more genes
    nsv6726188copy number variation1nstd229human GRCh38 chr3: 156,789,661-156,792,304 , GRCh37.p13 chr3: 156,507,450-156,510,093 LINC00886
    nsv6725393copy number variation1nstd229human GRCh38 chr3: 156,814,958-156,820,426 , GRCh37.p13 chr3: 156,532,747-156,538,215 LINC00886
    nsv6725189copy number variation1nstd229human GRCh38 chr3: 156,784,787-156,785,523 , GRCh37.p13 chr3: 156,502,576-156,503,312 LINC00886
    nsv6724729copy number variation1nstd229human GRCh38 chr3: 156,014,310-156,940,321 , GRCh37.p13 chr3: 155,732,099-156,658,110 ALG1L15P, SSR3, 12 more genes
    nsv6724655copy number variation1nstd229human GRCh38 chr3: 156,814,244-156,814,339 , GRCh37.p13 chr3: 156,532,033-156,532,128 LINC00886
    nsv6723767copy number variation1nstd229human GRCh38 chr3: 156,748,748-156,761,833 , GRCh37.p13 chr3: 156,466,537-156,479,622 LINC00886
    nsv6721977copy number variation1nstd229human GRCh38 chr3: 156,772,873-156,773,401 , GRCh37.p13 chr3: 156,490,662-156,491,190 LINC00886
    nsv6721954copy number variation1nstd229human GRCh38 chr3: 156,808,818-156,833,834 , GRCh37.p13 chr3: 156,526,607-156,551,623 LINC00886, LEKR1, 1 more genes
    nsv6719100copy number variation1nstd229human GRCh38 chr3: 156,763,401-156,770,800 , GRCh37.p13 chr3: 156,481,190-156,488,589 LINC00886
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