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Items: 1 to 20 of 193

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148081copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,167,260-12,533,766 , GRCh38.p12 chr3: 10,125,576-12,492,267 SLC6A1-AS1, LOC101927467, 37 more genes
    nsv7096925copy number variation1nstd102humanPathogenic GRCh37 chr3: 11,058,898-11,064,174 , GRCh38.p12 chr3: 11,017,212-11,022,488 SLC6A1-AS1, SLC6A1
    nsv7096924copy number variation1nstd102humanPathogenic GRCh37 chr3: 11,058,898-11,062,028 , GRCh38.p12 chr3: 11,017,212-11,020,342 SLC6A1, SLC6A1-AS1
    nsv7096528copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,094,051-11,078,652 , GRCh38.p12 chr3: 10,052,367-11,036,966 LINC00606, MIR378B, 19 more genes
    nsv7096434copy number variation1nstd102humanUncertain significance GRCh37 chr3: 11,075,305-11,078,652 , GRCh38.p12 chr3: 11,033,619-11,036,966 SLC6A1
    nsv7096433copy number variation1nstd102humanPathogenic GRCh37 chr3: 11,067,270-11,069,305 , GRCh38.p12 chr3: 11,025,584-11,027,619 SLC6A1
    nsv7055847inversion1nstd229human GRCh38 chr3: 5,111,802-11,290,661 , GRCh37.p13 chr3: 5,153,487-11,332,347 GHRLOS, LHFPL4, 96 more genes
    nsv7042755inversion1nstd229human GRCh38 chr3: 8,982,205-12,221,239 , GRCh37.p13 chr3: 9,023,889-12,262,739 SYN2, MTCO1P5, 74 more genes
    nsv6716115copy number variation1nstd229human GRCh38 chr3: 11,013,481-11,013,898 , GRCh37.p13 chr3: 11,055,167-11,055,584 SLC6A1-AS1, SLC6A1
    nsv6711057copy number variation1nstd229human GRCh38 chr3: 11,024,414-11,138,502 , GRCh37.p13 chr3: 11,066,100-11,180,188 LOC101927467, SLC6A1, 1 more genes
    nsv6706997copy number variation1nstd229human GRCh38 chr3: 11,020,508-11,020,682 , GRCh37.p13 chr3: 11,062,194-11,062,368 SLC6A1
    nsv6702567copy number variation1nstd229human GRCh38 chr3: 11,000,537-11,000,752 , GRCh37.p13 chr3: 11,042,223-11,042,438 SLC6A1
    nsv6637039copy number variation1nstd102humanPathogenic GRCh37 chr3: 10,024,917-11,917,048 , GRCh38.p12 chr3: 9,983,233-11,875,574 ATG7, GHRL, 35 more genes
    nsv6636276copy number variation1nstd102humanPathogenic GRCh37 chr3: 61,892-11,679,509 , GRCh38.p12 chr3: 20,214-11,638,035 RPL23AP39, LOC107986059, 144 more genes
    nsv6540919inversion1nstd223human GRCh38 chr3: 9,115,607-13,898,149 , GRCh37.p13 chr3: 9,157,291-13,939,646 MKRN2OS, RAF1, 106 more genes
    nsv6375371copy number variation1nstd223human GRCh38 chr3: 11,000,536-11,000,752 , GRCh37.p13 chr3: 11,042,222-11,042,438 SLC6A1
    nsv6363624copy number variation1nstd223human GRCh38 chr3: 10,991,501-10,993,200 , GRCh37.p13 chr3: 11,033,187-11,034,886 SLC6A1
    nsv6311883copy number variation1nstd102humanUncertain significance GRCh37 chr3: 7,782,024-11,078,652 , GRCh38.p12 chr3: 7,740,337-11,036,966 CIDECP1, LMCD1, 71 more genes
    nsv6311437copy number variation1nstd102humanUncertain significance GRCh37 chr3: 11,058,898-11,078,652 , GRCh38.p12 chr3: 11,017,212-11,036,966 SLC6A1-AS1, SLC6A1
    nsv6296103copy number variation1nstd186human GRCh37 chr3: 11,062,194-11,062,370 , GRCh38.p12 chr3: 11,020,508-11,020,684 SLC6A1
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