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Items: 1 to 20 of 968

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7145535insertion1nstd232human GRCh37.p13 chr2: 236,818,860-236,818,860 , GRCh38.p12 chr2: 235,910,216-235,910,216 AGAP1
    nsv7096621copy number variation1nstd102humanUncertain significance GRCh37 chr2: 236,403,331-237,032,766 , GRCh38.p12 chr2: 235,494,687-236,124,122 RN7SL204P, TMSB10P1, 5 more genes
    nsv7096405copy number variation1nstd102humanUncertain significance GRCh37 chr2: 236,949,375-237,032,766 , GRCh38.p12 chr2: 236,040,731-236,124,122 AGAP1, RN7SL204P
    nsv7096254copy number variation1nstd102humanUncertain significance GRCh37 chr2: 236,617,803-236,653,503 , GRCh38.p12 chr2: 235,709,159-235,744,859 LOC105373942, AGAP1
    nsv7096253copy number variation1nstd102humanUncertain significance GRCh37 chr2: 236,617,803-236,626,308 , GRCh38.p12 chr2: 235,709,159-235,717,664 AGAP1
    nsv7056978inversion1nstd229human GRCh38 chr2: 235,081,452-236,493,199 , GRCh37.p13 chr2: 235,990,096-237,401,842 LOC105373941, RNU7-127P, 14 more genes
    nsv7055553inversion1nstd229human GRCh38 chr2: 235,547,240-235,547,366 , GRCh37.p13 chr2: 236,455,884-236,456,010 AGAP1
    nsv7054987inversion1nstd229human GRCh38 chr2: 236,035,185-236,334,107 , GRCh37.p13 chr2: 236,943,829-237,242,750 RNU1-31P, RN7SL204P, 6 more genes
    nsv7054151inversion1nstd229human GRCh38 chr2: 235,508,479-235,520,686 , GRCh37.p13 chr2: 236,417,123-236,429,330 AGAP1, TNRC17
    nsv7052315inversion1nstd229human GRCh38 chr2: 235,721,119-235,727,431 , GRCh37.p13 chr2: 236,629,763-236,636,075 AGAP1
    nsv7052232inversion1nstd229human GRCh38 chr2: 235,543,847-235,547,027 , GRCh37.p13 chr2: 236,452,491-236,455,671 AGAP1
    nsv7049945inversion1nstd229human GRCh38 chr2: 236,120,533-236,120,614 , GRCh37.p13 chr2: 237,029,177-237,029,258 AGAP1
    nsv7047549inversion1nstd229human GRCh38 chr2: 236,010,287-240,118,231 , GRCh37.p13 chr2: 236,918,931-241,057,648 RAB17, COL6A3, 74 more genes
    nsv7045798inversion1nstd229human GRCh38 chr2: 235,721,285-235,888,028 , GRCh37.p13 chr2: 236,629,929-236,796,672 TMSB10P1, LOC105373942, 1 more genes
    nsv7044824inversion1nstd229human GRCh38 chr2: 235,546,348-235,549,938 , GRCh37.p13 chr2: 236,454,992-236,458,582 AGAP1
    nsv7042672inversion1nstd229human GRCh38 chr2: 236,070,810-236,092,670 , GRCh37.p13 chr2: 236,979,454-237,001,314 AGAP1, RN7SL204P
    nsv7042400inversion1nstd229human GRCh38 chr2: 235,946,991-235,948,821 , GRCh37.p13 chr2: 236,855,635-236,857,465 AGAP1
    nsv7041006inversion1nstd229human GRCh38 chr2: 235,834,851-235,846,451 , GRCh37.p13 chr2: 236,743,495-236,755,095 AGAP1
    nsv6718031copy number variation1nstd229human GRCh38 chr2: 235,936,593-235,940,318 , GRCh37.p13 chr2: 236,845,237-236,848,962 AGAP1
    nsv6717915copy number variation1nstd229human GRCh38 chr2: 235,511,267-235,513,679 , GRCh37.p13 chr2: 236,419,911-236,422,323 TNRC17, AGAP1
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