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Items: 1 to 20 of 158

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7140861insertion1nstd232human GRCh37.p13 chr2: 27,656,959-27,656,959 , GRCh38.p12 chr2: 27,434,092-27,434,092 NRBP1
    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
    nsv7046929inversion1nstd229human GRCh38 chr2: 27,161,080-28,820,407 , GRCh37.p13 chr2: 27,383,948-29,043,273 LOC100422227, PLB1, 54 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
    nsv6677985copy number variation1nstd229human GRCh38 chr2: 27,429,571-27,429,607 , GRCh37.p13 chr2: 27,652,438-27,652,474 NRBP1
    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
    nsv6670431copy number variation1nstd229human GRCh38 chr2: 27,423,081-27,426,249 , GRCh37.p13 chr2: 27,645,948-27,649,116 NRBP1
    nsv6665785copy number variation1nstd229human GRCh38 chr2: 27,430,180-27,430,330 , GRCh37.p13 chr2: 27,653,047-27,653,197 NRBP1
    nsv6662099copy number variation1nstd229human GRCh38 chr2: 27,414,225-27,426,504 , GRCh37.p13 chr2: 27,637,092-27,649,371 NRBP1
    nsv6661650copy number variation1nstd229human GRCh38 chr2: 27,435,327-27,494,660 , GRCh37.p13 chr2: 27,658,194-27,717,527 IFT172, KRTCAP3, 3 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
    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
    nsv6353756copy number variation1nstd223human GRCh38 chr2: 27,428,201-27,429,700 , GRCh37.p13 chr2: 27,651,068-27,652,567 NRBP1
    nsv6350721copy number variation1nstd223human GRCh38 chr2: 27,423,075-27,426,242 , GRCh37.p13 chr2: 27,645,942-27,649,109 NRBP1
    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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