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Items: 1 to 20 of 243

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097541copy number variation1nstd102humanPathogenic GRCh37 chr5: 68,715,213-68,737,481 , GRCh38.p12 chr5|NW_003315917.2: 202,809-224,623 , GRCh38.p12 chr5: 69,419,386-69,441,654 MARVELD2
    nsv7055630inversion1nstd229human GRCh38 chr5: 66,647,773-71,648,116 , GRCh37.p13 chr5: 65,943,601-70,943,943 OCLNP1, CDK7, 96 more genes
    nsv7046125inversion1nstd229human GRCh38 chr5: 69,199,477-71,010,577 , GRCh37.p13 chr5: 68,495,304-70,306,404 CDH12P3, LOC728488, 50 more genes
    nsv7045080inversion1nstd229human GRCh38 chr5: 67,733,468-69,446,994 , GRCh37.p13 chr5: 67,029,296-68,742,821 LOC105379013, KGD4, 31 more genes
    nsv7042302inversion1nstd229human GRCh38 chr5: 69,438,089-71,459,343 , GRCh37.p13 chr5: 68,733,916-70,755,170 LOC728499, LOC107986372, 53 more genes
    nsv6774700copy number variation1nstd229human GRCh38 chr5: 69,442,901-69,446,644 , GRCh37.p13 chr5: 68,738,728-68,742,471 MARVELD2
    nsv6771550copy number variation1nstd229human GRCh38 chr5: 69,428,201-69,428,600 , GRCh37.p13 chr5: 68,724,028-68,724,427 MARVELD2
    nsv6763618copy number variation1nstd229human GRCh38 chr5: 66,450,908-74,585,645 , GRCh37.p13 chr5: 65,746,736-73,881,470 LOC107986372, LOC105379027, 146 more genes
    nsv6760534copy number variation1nstd229human GRCh38 chr5: 69,415,604-69,451,263 , GRCh37.p13 chr5: 68,711,431-68,747,090 MARVELD2
    nsv6630789copy number variation1nstd224human GRCh37 chr5: 68,716,312-68,829,459 , GRCh38.p12 chr5: 69,420,485-69,533,632 , GRCh38.p12 chr5|NW_003315917.2: 203,908-316,576 MARVELD2, RPS27P14, 4 more genes
    nsv6571333inversion1nstd223human GRCh38 chr5: 69,413,392-69,413,578 , GRCh37.p13 chr5: 68,709,219-68,709,405 MARVELD2, RAD17
    nsv6568279inversion1nstd223human GRCh38 chr5: 69,439,201-69,439,687 , GRCh37.p13 chr5: 68,735,028-68,735,514 MARVELD2
    nsv6414131copy number variation1nstd223human GRCh38 chr5: 69,415,604-69,451,260 , GRCh37.p13 chr5: 68,711,431-68,747,087 MARVELD2
    nsv6408509copy number variation1nstd223human GRCh38 chr5: 69,428,160-69,428,670 , GRCh37.p13 chr5: 68,723,987-68,724,497 MARVELD2
    nsv6403312copy number variation1nstd223human GRCh38 chr5: 69,411,901-69,418,200 , GRCh37.p13 chr5: 68,707,728-68,714,027 MARVELD2, RAD17
    nsv6401282copy number variation1nstd223human GRCh38 chr5: 69,433,673-69,442,982 , GRCh37.p13 chr5: 68,729,500-68,738,809 MARVELD2
    nsv6313676copy number variation1nstd102humanPathogenic GRCh37 chr5: 64,049,692-70,306,646 , GRCh38.p12 chr5: 64,753,865-71,010,819 BCL9P1, CWC27, 105 more genes
    nsv6260475mobile element insertion1nstd215human GRCh38 chr5: 69,444,022-69,444,022 , GRCh37.p13 chr5: 68,739,849-68,739,849 MARVELD2
    nsv6135434copy number variation1nstd213human GRCh37 chr5: 68,330,000-69,000,001 , GRCh38.p12 chr5: 69,034,173-69,704,174 , GRCh38.p12 chr5|NW_003315917.2: 1-337,557 CCNB1, CDK7, 26 more genes
    nsv6135416copy number variation1nstd213human GRCh37 chr5: 50,510,000-68,870,001 , GRCh38.p12 chr5: 51,214,166-69,574,174 , TRIM23, 243 more genes
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