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Items: 1 to 20 of 145

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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
    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
    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
    nsv6667418copy number variation1nstd229human GRCh38 chr2: 26,758,538-26,901,747 , GRCh37.p13 chr2: 26,981,406-27,124,615 CDKN2AIPNLP2, CENPA, 2 more genes
    nsv6664059copy number variation1nstd229human GRCh38 chr2: 26,758,032-26,767,638 , GRCh37.p13 chr2: 26,980,900-26,990,506 SLC35F6
    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
    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
    nsv6351826copy number variation1nstd223human GRCh38 chr2: 26,779,640-26,784,080 , GRCh37.p13 chr2: 27,002,508-27,006,948 SLC35F6, CENPA
    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
    nsv6341048copy number variation1nstd223human GRCh38 chr2: 26,758,032-26,767,638 , GRCh37.p13 chr2: 26,980,900-26,990,506 SLC35F6
    nsv6339447copy number variation1nstd223human GRCh38 chr2: 26,781,721-26,782,639 , GRCh37.p13 chr2: 27,004,589-27,005,507 SLC35F6
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6290171copy number variation1nstd102humanUncertain significance GRCh37 chr2: 26,860,458-27,346,266 , GRCh38.p12 chr2: 26,637,590-27,123,398 AGBL5, RPL37P11, 16 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
    nsv5988829copy number variation1nstd212human GRCh38 chr2: 26,771,777-26,773,828 , GRCh37.p13 chr2: 26,994,645-26,996,696 SLC35F6
    nsv5876666copy number variation1nstd209human GRCh38 chr2: 26,771,777-26,773,828 , GRCh37.p13 chr2: 26,994,645-26,996,696 SLC35F6
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