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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099194copy number variation1nstd231human GRCh38.p12 chr1: 39,146,492-41,396,453 , GRCh37 chr1: 39,612,164-41,862,125 BMP8B, COL9A2, 65 more genes
    nsv7038879inversion1nstd229human GRCh38 chr1: 40,401,036-42,810,368 , GRCh37.p13 chr1: 40,866,708-43,276,039 CITED4, ZNF684, 53 more genes
    nsv6650120copy number variation1nstd229human GRCh38 chr1: 40,681,352-40,681,385 , GRCh37.p13 chr1: 41,147,024-41,147,057 RIMS3
    nsv6649910copy number variation1nstd229human GRCh38 chr1: 40,602,781-40,619,056 , GRCh37.p13 chr1: 41,068,453-41,084,728 RIMS3
    nsv6649391copy number variation1nstd229human GRCh38 chr1: 40,642,776-40,642,882 , GRCh37.p13 chr1: 41,108,448-41,108,554 RIMS3
    nsv6325006copy number variation1nstd223human GRCh38 chr1: 40,533,601-40,715,200 , GRCh37.p13 chr1: 40,999,273-41,180,872 NFYC, RIMS3, 6 more genes
    nsv6318839copy number variation1nstd223human GRCh38 chr1: 40,677,434-40,678,143 , GRCh37.p13 chr1: 41,143,106-41,143,815 RIMS3
    nsv6313688copy number variation1nstd102humanPathogenic GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139 LOC107984940, PPIAP36, 407 more genes
    nsv6313549copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 38,679,545-42,556,292 , GRCh38.p12 chr1: 38,213,873-42,090,621 BMP8B, COL9A2, 93 more genes
    nsv6299911copy number variation1nstd186human GRCh37 chr1: 41,128,878-41,128,977 , GRCh38.p12 chr1: 40,663,206-40,663,305 RIMS3, LOC105378675
    nsv6252530mobile element insertion1nstd215human GRCh38 chr1: 40,676,682-40,676,682 , GRCh37.p13 chr1: 41,142,354-41,142,354 RIMS3
    nsv6158936copy number variation1nstd214human GRCh38 chr1: 40,642,776-40,642,881 , GRCh37.p13 chr1: 41,108,448-41,108,553 RIMS3
    nsv6133994copy number variation1nstd213human GRCh37 chr1: 37,480,000-43,930,001 , GRCh38.p12 chr1: 37,014,399-43,464,330 BMP8B, CDC20, 183 more genes
    nsv5984328copy number variation1nstd212human GRCh38 chr1: 40,642,776-40,642,882 , GRCh37.p13 chr1: 41,108,448-41,108,554 RIMS3
    nsv5879274copy number variation1nstd209human GRCh38 chr1: 40,642,776-40,642,881 , GRCh37.p13 chr1: 41,108,448-41,108,553 RIMS3
    nsv5693304mobile element insertion1nstd211human GRCh38 chr1: 40,679,618-40,679,618 , GRCh37.p13 chr1: 41,145,290-41,145,290 RIMS3
    nsv5575974copy number variation1nstd207human GRCh38 chr1: 40,642,776-40,642,881 , GRCh37.p13 chr1: 41,108,448-41,108,553 RIMS3
    nsv5433235copy number variation1nstd206human GRCh38 chr1: 40,663,206-40,663,305 , GRCh37.p13 chr1: 41,128,878-41,128,977 RIMS3, LOC105378675
    nsv5433191copy number variation1nstd206human GRCh38 chr1: 40,661,791-40,663,663 , GRCh37.p13 chr1: 41,127,463-41,129,335 RIMS3, LOC105378675
    nsv5432251copy number variation1nstd206human GRCh38 chr1: 40,655,291-40,655,718 , GRCh37.p13 chr1: 41,120,963-41,121,390 RIMS3
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