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Items: 1 to 20 of 204

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7098835copy number variation1nstd102humanPathogenic GRCh37 chr4: 88,344,058-89,061,168 , GRCh38.p12 chr4: 87,422,906-88,140,016 SPARCL1, DSPP, 13 more genes
    nsv7057926inversion1nstd229human GRCh38 chr4: 87,164,841-87,871,077 , GRCh37.p13 chr4: 88,085,993-88,792,229 MIR5705, DSPP, 16 more genes
    nsv7054126inversion1nstd229human GRCh38 chr4: 87,165,000-87,871,044 , GRCh37.p13 chr4: 88,086,152-88,792,196 SCPPPQ1, LOC100129693, 16 more genes
    nsv7053706inversion1nstd229human GRCh38 chr4: 87,843,889-87,850,103 , GRCh37.p13 chr4: 88,765,041-88,771,255 MEPE
    nsv7053656inversion1nstd229human GRCh38 chr4: 86,694,351-88,137,907 , GRCh37.p13 chr4: 87,615,504-89,059,059 KLHL8, GAPDHP60, 30 more genes
    nsv7050046inversion1nstd229human GRCh38 chr4: 85,500,769-88,545,032 , GRCh37.p13 chr4: 86,421,922-89,466,183 LOC105377326, NUDT9, 54 more genes
    nsv6757390copy number variation1nstd229human GRCh38 chr4: 87,839,001-87,843,600 , GRCh37.p13 chr4: 88,760,153-88,764,752 MEPE
    nsv6749121copy number variation1nstd229human GRCh38 chr4: 87,071,740-88,273,767 , GRCh37.p13 chr4: 87,992,892-89,194,919 RNU6-818P, DMP1, 29 more genes
    nsv6746802copy number variation1nstd229human GRCh38 chr4: 87,682,577-87,870,070 , GRCh37.p13 chr4: 88,603,729-88,791,222 MEPE, CHCHD2P7, 2 more genes
    nsv6739317copy number variation1nstd229human GRCh38 chr4: 87,822,691-87,828,248 , GRCh37.p13 chr4: 88,743,843-88,749,400 MEPE
    nsv6739225copy number variation1nstd229human GRCh38 chr4: 87,772,406-87,847,336 , GRCh37.p13 chr4: 88,693,558-88,768,488 IBSP, MEPE, 1 more genes
    nsv6636515copy number variation1nstd102humanUncertain significance GRCh37 chr4: 88,696,112-88,764,990 , GRCh38.p12 chr4: 87,774,960-87,843,838 IBSP, MEPE, 1 more genes
    nsv6561923inversion1nstd223human GRCh38 chr4: 87,824,340-87,825,235 , GRCh37.p13 chr4: 88,745,492-88,746,387 MEPE
    nsv6393987copy number variation1nstd223human GRCh38 chr4: 87,846,280-87,846,995 , GRCh37.p13 chr4: 88,767,432-88,768,147 MEPE
    nsv6376153copy number variation1nstd223human GRCh38 chr4: 87,846,896-87,847,307 , GRCh37.p13 chr4: 88,768,048-88,768,459 MEPE
    nsv6313848copy number variation1nstd102humanPathogenic GRCh37 chr4: 81,054,789-90,667,421 , GRCh38.p12 chr4: 80,133,635-89,746,270 RPL6P13, SNORD144, 136 more genes
    nsv6313510copy number variation1nstd102humanPathogenic GRCh37 chr4: 75,737,340-91,131,156 , GRCh38.p12 chr4: 74,812,130-90,210,005 HIGD1AP13, CXCL11, 240 more genes
    nsv6313484copy number variation1nstd102humanPathogenic GRCh37 chr4: 79,780,152-94,873,225 , GRCh38.p12 chr4: 78,858,998-93,952,074 LOC105377329, LOC107986294, 166 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
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