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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096625copy number variation1nstd102humanUncertain significance GRCh37 chr2: 24,443,763-30,143,525 , GRCh38.p12 chr2: 24,220,894-29,920,659 LOC105374381, POMC, 136 more genes
    nsv7096491copy number variation1nstd102humanUncertain significance GRCh37 chr2: 27,275,827-27,457,573 , GRCh38.p12 chr2: 27,052,959-27,234,705 PRR30, TCF23, 10 more genes
    nsv7096148copy number variation2nstd102humanUncertain significance GRCh37 chr2: 24,443,763-29,022,169 , GRCh38.p12 chr2: 24,220,894-28,799,303 LOC105374381, SLC35F6, 122 more genes
    nsv7042984inversion1nstd229human GRCh38 chr2: 26,886,657-32,818,427 , GRCh37.p13 chr2: 27,109,525-33,043,494 CLIP4, LOC102723594, 118 more genes
    nsv6672785copy number variation1nstd229human GRCh38 chr2: 24,384,939-32,866,867 , GRCh37.p13 chr2: 24,607,808-33,091,934 CENPO, TOGARAM2, 170 more genes
    nsv6662597copy number variation1nstd229human GRCh38 chr2: 27,057,801-27,141,300 , GRCh37.p13 chr2: 27,280,669-27,364,168 AGBL5, KHK, 6 more genes
    nsv6659379copy number variation1nstd229human GRCh38 chr2: 27,133,401-27,137,800 , GRCh37.p13 chr2: 27,356,269-27,360,668 PRR30, PREB
    nsv6636815copy number variation1nstd102humanPathogenic GRCh37 chr2: 706,460-35,523,639 , GRCh38.p12 chr2: 706,460-35,298,573 LOC105374455, RN7SL674P, 504 more genes
    nsv6634330copy number variation1nstd102humanPathogenic GRCh37 chr2: 11,504,318-111,365,996 , GRCh38.p12 chr2: 11,364,192-110,608,419 CYP1B1-AS1, LOC107985771, 1649 more genes
    nsv6628047copy number variation1nstd224human GRCh37 chr2: 27,290,373-27,384,579 , GRCh38.p12 chr2: 27,067,505-27,161,711 KHK, PREB, 7 more genes
    nsv6546927inversion1nstd223human GRCh38 chr2: 26,476,473-32,916,584 , GRCh37.p13 chr2: 26,699,341-33,141,651 LOC105374453, LCLAT1, 129 more genes
    nsv6543735inversion1nstd223human GRCh38 chr2: 24,403,241-32,916,237 , GRCh37.p13 chr2: 24,626,110-33,141,304 LOC105374334, LOC107985861, 172 more genes
    nsv6538559inversion1nstd223human GRCh38 chr2: 25,762,333-32,867,002 , GRCh37.p13 chr2: 25,985,202-33,092,069 MIR558, PCARE, 148 more genes
    nsv6355117copy number variation1nstd223human GRCh38 chr2: 27,127,401-27,132,400 , GRCh37.p13 chr2: 27,350,269-27,355,268 ABHD1, PREB
    nsv6344534copy number variation1nstd223human GRCh38 chr2: 24,831,925-32,916,230 , GRCh37.p13 chr2: 25,054,794-33,141,297 LOC102723594, DNAJC5G, 165 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6137788copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,601,818-43,466,284 , GRCh38.p12 chr2: 24,378,949-43,239,145 GTF3C2-AS1, MAPRE3-AS1, 316 more genes
    nsv6112680copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 24,881,528-43,460,021 , GRCh38.p12 chr2: 24,658,659-43,232,882 ADCY3, ALK, 314 more genes
    nsv5358748translocation1nstd200human GRCh38 chr2: 27,134,918-27,134,918 , GRCh38 chr2: 27,134,391-27,134,391 , GRCh37.p13 chr2: 27,357,786-27,357,786 , GRCh37.p13 chr2: 27,357,259-27,357,259 PRR30, PREB
    nsv4900787copy number variation1nstd200human GRCh38 chr2: 27,127,503-27,131,967 , GRCh37.p13 chr2: 27,350,371-27,354,835 ABHD1, PREB
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