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Items: 1 to 20 of 402

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096653copy number variation1nstd102humanUncertain significance GRCh37 chr2: 38,121,051-47,710,088 , GRCh38.p12 chr2: 37,893,908-47,482,949 PLEKHH2, RNU6-566P, 151 more genes
    nsv7096652copy number variation1nstd102humanPathogenic GRCh37 chr2: 37,334,416-39,347,563 , GRCh38.p12 chr2: 37,107,273-39,120,422 RPL31P16, GALM, 52 more genes
    nsv7096503copy number variation1nstd102humanPathogenic GRCh37 chr2: 38,297,865-38,917,056 , GRCh38.p12 chr2: 38,070,722-38,689,914 CYP1B1, CYP1B1-AS1, 13 more genes
    nsv7057097inversion1nstd229human GRCh38 chr2: 37,932,079-38,404,442 , GRCh37.p13 chr2: 38,159,222-38,631,584 RPL7P12, RMDN2-AS1, 10 more genes
    nsv7047226inversion1nstd229human GRCh38 chr2: 37,930,912-38,404,421 , GRCh37.p13 chr2: 38,158,055-38,631,563 LOC107985871, LOC105374467, 10 more genes
    nsv7041239inversion1nstd229human GRCh38 chr2: 38,342,909-38,353,044 , GRCh37.p13 chr2: 38,570,051-38,580,186 ATL2
    nsv6675541copy number variation1nstd229human GRCh38 chr2: 38,300,628-38,302,662 , GRCh37.p13 chr2: 38,527,770-38,529,804 ATL2
    nsv6675259copy number variation1nstd229human GRCh38 chr2: 38,332,523-38,332,597 , GRCh37.p13 chr2: 38,559,665-38,559,739 ATL2
    nsv6673033copy number variation1nstd229human GRCh38 chr2: 38,368,459-38,368,526 , GRCh37.p13 chr2: 38,595,601-38,595,668 ATL2
    nsv6672321copy number variation1nstd229human GRCh38 chr2: 38,347,701-38,432,100 , GRCh37.p13 chr2: 38,574,843-38,659,242 LINC01883, LOC105374468, 1 more genes
    nsv6670798copy number variation1nstd229human GRCh38 chr2: 38,353,898-38,354,267 , GRCh37.p13 chr2: 38,581,040-38,581,409 ATL2
    nsv6670556copy number variation1nstd229human GRCh38 chr2: 38,267,997-38,304,455 , GRCh37.p13 chr2: 38,495,139-38,531,597 ATL2, GAPDHP25, 1 more genes
    nsv6669891copy number variation1nstd229human GRCh38 chr2: 38,344,301-38,417,300 , GRCh37.p13 chr2: 38,571,443-38,644,442 LOC105374468, ATL2
    nsv6666459copy number variation1nstd229human GRCh38 chr2: 38,329,901-38,338,700 , GRCh37.p13 chr2: 38,557,043-38,565,842 ATL2
    nsv6665096copy number variation1nstd229human GRCh38 chr2: 38,353,001-38,368,300 , GRCh37.p13 chr2: 38,580,143-38,595,442 ATL2
    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
    nsv6627847copy number variation1nstd224human GRCh37 chr2: 38,316,571-38,580,233 , GRCh38.p12 chr2: 38,089,429-38,353,091 ATL2, CYP1B1-AS1, 6 more genes
    nsv6554157inversion1nstd223human GRCh38 chr2: 38,360,109-38,360,259 , GRCh37.p13 chr2: 38,587,251-38,587,401 ATL2
    nsv6553128inversion1nstd223human GRCh38 chr2: 38,351,556-38,352,124 , GRCh37.p13 chr2: 38,578,698-38,579,266 ATL2
    nsv6552570inversion1nstd223human GRCh38 chr2: 38,339,219-38,339,712 , GRCh37.p13 chr2: 38,566,361-38,566,854 ATL2
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