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Items: 1 to 20 of 169

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098853copy number variation1nstd102humanUncertain significance GRCh37 chr2: 24,962,301-26,257,604 , GRCh38.p12 chr2: 24,739,432-26,034,735 TPM3P7, EFR3B, 25 more genes
    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
    nsv7096411copy number variation1nstd102humanPathogenic GRCh37 chr2: 24,443,763-26,029,226 , GRCh38.p12 chr2: 24,220,894-25,806,357 LOC105369164, DTNB-AS1, 24 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
    nsv7056460inversion1nstd229human GRCh38 chr2: 25,346,186-25,553,075 , GRCh37.p13 chr2: 25,569,055-25,775,944 DTNB-AS1, DTNB
    nsv7051652inversion1nstd229human GRCh38 chr2: 25,346,353-25,549,724 , GRCh37.p13 chr2: 25,569,222-25,772,593 DTNB-AS1, DTNB
    nsv7047614inversion1nstd229human GRCh38 chr2: 25,421,845-25,421,938 , GRCh37.p13 chr2: 25,644,714-25,644,807 DTNB, DTNB-AS1
    nsv6674659copy number variation1nstd229human GRCh38 chr2: 25,435,275-25,438,913 , GRCh37.p13 chr2: 25,658,144-25,661,782 DTNB, DTNB-AS1
    nsv6674629copy number variation1nstd229human GRCh38 chr2: 24,323,879-25,622,192 , GRCh37.p13 chr2: 24,546,748-25,845,061 POMC, RNA5SP88, 22 more genes
    nsv6674443copy number variation1nstd229human GRCh38 chr2: 25,423,754-25,432,285 , GRCh37.p13 chr2: 25,646,623-25,655,154 DTNB-AS1, DTNB
    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
    nsv6669803copy number variation1nstd229human GRCh38 chr2: 25,006,601-25,432,200 , GRCh37.p13 chr2: 25,229,470-25,655,069 LINC01381, DTNB-AS1, 8 more genes
    nsv6666925copy number variation1nstd229human GRCh38 chr2: 25,387,201-25,429,200 , GRCh37.p13 chr2: 25,610,070-25,652,069 DTNB-AS1, DTNB
    nsv6664717copy number variation1nstd229human GRCh38 chr2: 25,227,058-26,008,194 , GRCh37.p13 chr2: 25,449,927-26,231,063 TPM3P7, MIR1301, 9 more genes
    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
    nsv6543735inversion1nstd223human GRCh38 chr2: 24,403,241-32,916,237 , GRCh37.p13 chr2: 24,626,110-33,141,304 LOC105374334, LOC107985861, 172 more genes
    nsv6538674inversion1nstd223human GRCh38 chr2: 25,436,064-25,437,550 , GRCh37.p13 chr2: 25,658,933-25,660,419 DTNB-AS1, DTNB
    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
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