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Items: 1 to 20 of 333

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096527copy number variation1nstd102humanUncertain significance GRCh37 chr2: 97,462,729-97,475,254 , GRCh38.p12 chr2: 96,796,992-96,809,517 CNNM4, MIR3127
    nsv7093448delins1nstd102humanUncertain significance GRCh38 chr2: 96,808,762-96,809,378 , GRCh37 chr2: 97,474,499-97,475,115 CNNM4
    nsv6695059copy number variation1nstd229human GRCh38 chr2: 96,765,101-96,769,100 , GRCh37.p13 chr2: 97,430,838-97,434,837 CNNM4
    nsv6687923copy number variation1nstd229human GRCh38 chr2: 96,775,984-96,781,238 , GRCh37.p13 chr2: 97,441,721-97,446,975 CNNM4
    nsv6687406copy number variation1nstd229human GRCh38 chr2: 96,767,825-96,768,032 , GRCh37.p13 chr2: 97,433,562-97,433,769 CNNM4
    nsv6684680copy number variation1nstd229human GRCh38 chr2: 96,759,540-96,759,691 , GRCh37.p13 chr2: 97,425,277-97,425,428 CNNM4
    nsv6683787copy number variation1nstd229human GRCh38 chr2: 96,799,201-96,805,400 , GRCh37.p13 chr2: 97,464,938-97,471,137 CNNM4
    nsv6683050copy number variation1nstd229human GRCh38 chr2: 96,764,687-96,769,172 , GRCh37.p13 chr2: 97,430,424-97,434,909 CNNM4
    nsv6682075copy number variation1nstd229human GRCh38 chr2: 96,753,801-96,759,200 , GRCh37.p13 chr2: 97,419,538-97,424,937 CNNM4
    nsv6636315copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 95,341,388-100,340,514 , GRCh38.p12 chr2: 94,675,663-99,724,052 ADRA2B, ATP5F1BP1, 130 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
    nsv6628429copy number variation1nstd224human GRCh37 chr2: 96,747,466-98,186,298 , GRCh38.p12 chr2: 96,081,718-97,569,835 ARID5A, IGKV2OR2-2, 42 more genes
    nsv6628179copy number variation1nstd224human GRCh37 chr2: 96,721,808-98,186,298 , GRCh38.p12 chr2: 96,056,060-97,569,835 ADRA2B, IGKV2OR2-10, 43 more genes
    nsv6554656inversion1nstd223human GRCh38 chr2: 96,790,442-96,791,709 , GRCh37.p13 chr2: 97,456,179-97,457,446 CNNM4
    nsv6552788inversion1nstd223human GRCh38 chr2: 96,785,117-96,785,285 , GRCh37.p13 chr2: 97,450,854-97,451,022 CNNM4
    nsv6547092inversion1nstd223human GRCh38 chr2: 96,007,660-97,097,743 , GRCh37.p13 chr2: 96,673,408-97,763,480 CNNM4, DUSP2, 34 more genes
    nsv6546977inversion1nstd223human GRCh38 chr2: 96,774,986-96,776,046 , GRCh37.p13 chr2: 97,440,723-97,441,783 CNNM4
    nsv6347687copy number variation1nstd223human GRCh38 chr2: 96,748,071-96,773,622 , GRCh37.p13 chr2: 97,413,808-97,439,359 CNNM4
    nsv6346839copy number variation1nstd223human GRCh38 chr2: 96,730,906-96,781,234 , GRCh37.p13 chr2: 97,396,643-97,446,971 CNNM4, LMAN2L
    nsv6345485copy number variation1nstd223human GRCh38 chr2: 96,768,901-96,777,800 , GRCh37.p13 chr2: 97,434,638-97,443,537 CNNM4
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