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Items: 1 to 20 of 413

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7047138inversion1nstd229human GRCh38 chr2: 241,752,746-241,987,074 , GRCh37.p13 chr2: 242,692,161-242,929,225 LINC01238, RTP5, 9 more genes
    nsv7038542inversion1nstd229human GRCh38 chr2: 241,831,979-242,023,703 , GRCh37.p13 chr2: 242,774,156-242,965,854 FAM240C, LINC01238, 6 more genes
    nsv6717538copy number variation1nstd229human GRCh38 chr2: 241,801,948-242,059,511 , GRCh37.p13 chr2: 242,741,363-243,001,662 LOC107986004, LINC01880, 11 more genes
    nsv6714991copy number variation1nstd229human GRCh38 chr2: 241,860,166-241,897,172 , GRCh37.p13 chr2: 242,802,318-242,839,323 FAM240C, LINC01237, 2 more genes
    nsv6711989copy number variation1nstd229human GRCh38 chr2: 241,731,561-241,908,453 , GRCh37.p13 chr2: 242,670,976-242,850,604 GAL3ST2, PDCD1, 8 more genes
    nsv6708729copy number variation1nstd229human GRCh38 chr2: 241,867,501-241,888,200 , GRCh37.p13 chr2: 242,809,653-242,830,351 LOC105373978, LINC01237, 1 more genes
    nsv6707329copy number variation1nstd229human GRCh38 chr2: 241,709,883-241,892,927 , GRCh37.p13 chr2: 242,649,298-242,835,078 D2HGDH, LINC01237, 9 more genes
    nsv6705507copy number variation1nstd229human GRCh38 chr2: 241,854,772-242,033,580 , GRCh37.p13 chr2: 242,796,924-242,975,731 LOC285097, LINC01237, 6 more genes
    nsv6702834copy number variation1nstd229human GRCh38 chr2: 241,795,001-242,003,800 , GRCh37.p13 chr2: 242,734,416-242,945,951 GAL3ST2, LOC105373978, 9 more genes
    nsv6698745copy number variation1nstd229human GRCh38 chr2: 241,795,701-241,911,700 , GRCh37.p13 chr2: 242,735,116-242,853,851 GAL3ST2, NEU4, 7 more genes
    nsv6635745copy number variation2nstd227human GRCh38.p12 chr2: 241,869,928-242,106,609 , GRCh37 chr2: 242,812,080-243,048,760 , GRCh38.p12 chr2|NT_187647.1: 1-150,319 , GRCh38.p12 chr2|NT_187523.1: 1-150,679 RTP5, FAM240C, 7 more genes
    nsv6635655copy number variation1nstd227human GRCh37 chr2: 242,795,942-243,048,760 , GRCh38.p12 chr2: 241,853,790-242,106,609 , GRCh38.p12 chr2|NT_187523.1: 1-150,679 , GRCh38.p12 chr2|NT_187647.1: 1-150,319 PDCD1, RTP5, 9 more genes
    nsv6635019copy number variation2nstd227human GRCh37 chr2: 242,795,350-243,048,760 , GRCh38.p12 chr2: 241,853,198-242,106,609 , GRCh38.p12 chr2|NT_187523.1: 1-150,679 , GRCh38.p12 chr2|NT_187647.1: 1-150,319 PDCD1, RTP5, 9 more genes
    nsv6634860copy number variation1nstd227human GRCh37 chr2: 242,763,542-243,048,760 , GRCh38.p12 chr2: 241,821,357-242,106,609 , GRCh38.p12 chr2|NT_187523.1: 1-150,679 , GRCh38.p12 chr2|NT_187647.1: 1-150,319 PDCD1, RTP5, 10 more genes
    nsv6634398copy number variation1nstd102humanPathogenic GRCh37 chr2: 239,229,304-243,199,373 , GRCh38.p12 chr2: 238,320,663-242,157,305 HDAC4-AS1, ING5, 92 more genes
    nsv6628087copy number variation1nstd224human GRCh37 chr2: 242,814,705-243,034,519 , GRCh38.p12 chr2: 241,872,553-242,092,368 , GRCh38.p12 chr2|NT_187523.1: 1-136,438 , GRCh38.p12 chr2|NT_187647.1: 1-136,078 RTP5, FAM240C, 7 more genes
    nsv6628032copy number variation1nstd224human GRCh37 chr2: 242,794,796-243,034,519 , GRCh38.p12 chr2: 241,852,644-242,092,368 , GRCh38.p12 chr2|NT_187523.1: 1-136,438 , GRCh38.p12 chr2|NT_187647.1: 1-136,078 LOC285097, LINC01237, 9 more genes
    nsv6628031copy number variation1nstd224human GRCh37 chr2: 242,793,290-242,824,974 , GRCh38.p12 chr2: 241,851,138-241,882,823 , GRCh38.p12 chr2|NT_187527.1: 63,236-94,921 LOC105373977, RTP5, 3 more genes
    nsv6627658copy number variation1nstd224human GRCh37 chr2: 242,814,983-243,034,519 , GRCh38.p12 chr2: 241,872,831-242,092,368 , GRCh38.p12 chr2|NT_187523.1: 1-136,438 , GRCh38.p12 chr2|NT_187647.1: 1-136,078 RTP5, FAM240C, 7 more genes
    nsv6627657copy number variation2nstd224human GRCh37 chr2: 242,814,758-243,034,519 , GRCh38.p12 chr2: 241,872,606-242,092,368 , GRCh38.p12 chr2|NT_187523.1: 1-136,438 , GRCh38.p12 chr2|NT_187647.1: 1-136,078 RTP5, FAM240C, 7 more genes
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