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Items: 1 to 20 of 524

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097629copy number variation1nstd102humanUncertain significance GRCh37 chr7: 44,298,451-44,365,020 , GRCh38.p12 chr7: 44,258,852-44,325,421 CAMK2B
    nsv7097628copy number variation1nstd102humanUncertain significance GRCh37 chr7: 44,153,173-44,365,020 , GRCh38.p12 chr7: 44,113,574-44,325,421 LOC105375257, AEBP1, 7 more genes
    nsv7097375copy number variation1nstd102humanUncertain significance GRCh37 chr7: 43,810,758-44,747,598 , GRCh38.p12 chr7: 43,771,159-44,707,999 RASA4CP, OGDH, 31 more genes
    nsv7040618inversion1nstd229human GRCh38 chr7: 44,326,115-44,326,174 , GRCh37.p13 chr7: 44,365,714-44,365,773 CAMK2B
    nsv6837691copy number variation1nstd229human GRCh38 chr7: 44,221,432-44,221,560 , GRCh37.p13 chr7: 44,261,031-44,261,159 CAMK2B
    nsv6834700copy number variation1nstd229human GRCh38 chr7: 44,125,000-44,232,183 , GRCh37.p13 chr7: 44,164,599-44,271,782 CAMK2B, GCK, 5 more genes
    nsv6830685copy number variation1nstd229human GRCh38 chr7: 44,270,492-44,401,477 , GRCh37.p13 chr7: 44,310,091-44,441,076 NUDCD3, CAMK2B
    nsv6827396copy number variation1nstd229human GRCh38 chr7: 44,289,843-44,292,626 , GRCh37.p13 chr7: 44,329,442-44,332,225 CAMK2B
    nsv6824678copy number variation1nstd229human GRCh38 chr7: 44,223,824-44,224,004 , GRCh37.p13 chr7: 44,263,423-44,263,603 CAMK2B
    nsv6824624copy number variation1nstd229human GRCh38 chr7: 44,259,520-44,259,693 , GRCh37.p13 chr7: 44,299,119-44,299,292 CAMK2B
    nsv6824378copy number variation1nstd229human GRCh38 chr7: 43,852,301-44,460,500 , GRCh37.p13 chr7: 43,891,900-44,500,099 DBNL, GCK, 23 more genes
    nsv6823138copy number variation1nstd229human GRCh38 chr7: 44,236,956-44,237,196 , GRCh37.p13 chr7: 44,276,555-44,276,795 CAMK2B
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6607568copy number variation1nstd223human GRCh38 chr7: 44,221,430-44,221,560 , GRCh37.p13 chr7: 44,261,029-44,261,159 CAMK2B
    nsv6604714copy number variation1nstd223human GRCh38 chr7: 44,313,819-44,319,283 , GRCh37.p13 chr7: 44,353,418-44,358,882 CAMK2B
    nsv6574607inversion1nstd223human GRCh38 chr7: 35,958,610-45,735,691 , GRCh37.p13 chr7: 35,998,220-45,775,290 RPS17P13, LOC105375252, 182 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313509copy number variation1nstd102humanPathogenic GRCh37 chr7: 40,778,439-50,228,656 , GRCh38.p12 chr7: 40,738,840-50,189,060 LINC01447, ABCA13, 142 more genes
    nsv6312348copy number variation1nstd102humanUncertain significance GRCh37 chr7: 44,266,210-44,268,489 , GRCh38.p12 chr7: 44,226,611-44,228,890 CAMK2B
    nsv6301780copy number variation1nstd186human GRCh37 chr7: 44,268,459-44,269,036 , GRCh38.p12 chr7: 44,228,860-44,229,437 CAMK2B
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