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Items: 1 to 20 of 121

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6553936inversion1nstd223human GRCh38 chr2: 86,913,704-87,825,694 , GRCh37.p13 chr2: 87,140,827-88,125,213 ANAPC1P2, CYTOR, 27 more genes
    nsv6547455inversion1nstd223human GRCh38 chr2: 86,913,968-87,825,588 , GRCh37.p13 chr2: 87,141,091-88,125,107 DBF4P3, LOC102724642, 27 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6314726copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 40,607,042-146,902,764 , GRCh38.p12 chr2: 40,379,902-146,145,196 ACTG2, ACYP2, 1713 more genes
    nsv6313890copy number variation1nstd102humanPathogenic GRCh37 chr2: 82,486,900-87,322,042 , GRCh38.p12 chr2: 82,259,776-87,094,919 LOC105374836, LOC105374833, 93 more genes
    nsv5554214mobile element insertion1nstd206human GRCh38 chr2: 43,826,578-177,947,868 , GRCh37.p13 chr2: 44,053,717-178,812,595 , POLR1B, 2149 more genes
    nsv5436982copy number variation1nstd206human GRCh38 chr2: 85,539,948-89,142,574 , GRCh37.p13 chr2: 85,767,071-89,442,057 , IGKV2-18, 129 more genes
    nsv5210910copy number variation1nstd204human GRCh38.p13 chr2: 87,010,701-87,013,700 , GRCh37.p13 chr2: 87,237,824-87,240,823 RGPD1, PLGLB1
    nsv5035923inversion1nstd200human GRCh38 chr2: 83,726,586-172,391,178 , GRCh37.p13 chr2: 83,953,710-173,255,906 , MTND2P21, 1427 more genes
    nsv4679934copy number variation1nstd189human GRCh37.p13 chr2: 87,120,496-88,024,667 , GRCh38.p12 chr2: 86,893,373-87,725,148 , PLGLB1, 26 more genes
    nsv4665541copy number variation1nstd186human GRCh37 chr2: 87,243,379-87,243,450 , GRCh38.p12 chr2: 87,016,256-87,016,327 PLGLB1
    nsv4663386copy number variation1nstd186human GRCh37 chr2: 87,159,729-88,004,998 , GRCh38.p12 chr2: 86,932,606-87,705,479 , PAFAH1B1P1, 24 more genes
    nsv4656532copy number variation1nstd186human GRCh37 chr2: 87,242,200-87,253,600 , GRCh38.p12 chr2: 87,015,077-87,026,477 PLGLB1
    nsv4584604copy number variation2nstd183human GRCh37 chr2: 87,159,729-88,004,998 , GRCh38.p12 chr2: 86,932,606-87,705,479 , ANAPC1P3, 24 more genes
    nsv4584603copy number variation1nstd183human GRCh37 chr2: 87,089,683-87,376,944 , GRCh38.p12 chr2: 86,862,560-87,149,821 , TRP-AGG4-1, 8 more genes
    nsv4584246copy number variation1nstd183human GRCh37 chr2: 87,243,379-87,243,450 , GRCh38.p12 chr2: 87,016,256-87,016,327 PLGLB1
    nsv4519695copy number variation1nstd166human GRCh37.p13 chr2: 85,888,999-87,236,000 , GRCh38.p12 chr2: 85,661,876-87,008,877 , RNF103, 33 more genes
    nsv4451607copy number variation1nstd102humanPathogenic GRCh37 chr2: 77,907,114-87,330,965 , GRCh38.p12 chr2: 77,679,988-87,103,842 REEP1, RBX1P1, 134 more genes
    nsv4397973copy number variation1nstd174human GRCh37 chr2: 87,105,444-88,310,990 , GRCh38.p12 chr2: 86,878,321-88,011,471 , PLGLB1, 35 more genes
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