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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148254copy number variation1nstd102humanPathogenic GRCh38 chr17: 165,730-11,404,096 , GRCh37.p13 chr17: 396,627-11,307,413 RFLNB, C17orf100, 401 more genes
    nsv7098895copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,004,894-7,766,789 , GRCh38.p12 chr17: 7,101,575-7,863,471 LOC105371512, EIF4A1, 61 more genes
    nsv7095414copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,123,304-8,193,254 , GRCh38.p12 chr17: 7,219,985-8,289,936 CTC1, SAT2, 103 more genes
    nsv7095413copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,123,304-7,606,804 , GRCh38.p12 chr17: 7,219,985-7,703,486 MPDU1, PLSCR3, 50 more genes
    nsv7095410copy number variation2nstd102humanUncertain significance GRCh37 chr17: 6,328,780-7,606,804 , GRCh38.p12 chr17: 6,425,460-7,703,486 PITPNM3, SLC2A4, 85 more genes
    nsv7094915copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,120,455-8,151,423 , GRCh38.p12 chr17: 7,217,136-8,248,105 MIR324, SLC2A4, 101 more genes
    nsv7073912inversion1nstd229human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 TNFSF12, SCARNA21, 321 more genes
    nsv7073657inversion1nstd229human GRCh38 chr17: 3,848,628-8,774,303 , GRCh37.p13 chr17: 3,751,922-8,677,621 LOC107987245, TRI-AAT5-5, 243 more genes
    nsv6996324copy number variation1nstd229human GRCh38 chr17: 7,248,612-7,248,676 , GRCh37.p13 chr17: 7,151,931-7,151,995 CTDNEP1
    nsv6995956copy number variation1nstd229human GRCh38 chr17: 7,211,801-7,562,200 , GRCh37.p13 chr17: 7,115,120-7,465,517 DVL2, SPEM2, 34 more genes
    nsv6993452copy number variation1nstd229human GRCh38 chr17: 7,243,196-7,243,222 , GRCh37.p13 chr17: 7,146,515-7,146,541 CTDNEP1
    nsv6989012copy number variation1nstd229human GRCh38 chr17: 7,237,301-7,244,200 , GRCh37.p13 chr17: 7,140,620-7,147,519 CTDNEP1, PHF23, 1 more genes
    nsv6984865copy number variation1nstd229human GRCh38 chr17: 7,247,719-7,265,990 , GRCh37.p13 chr17: 7,151,038-7,169,309 CTDNEP1, CLDN7, 1 more genes
    nsv6982450copy number variation1nstd229human GRCh38 chr17: 1,838,614-7,660,509 , GRCh37.p13 chr17: 1,741,908-7,563,827 NCBP3, OR1P1, 242 more genes
    nsv6637921copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,043,719-7,193,448 , GRCh38.p12 chr17: 7,140,400-7,290,129 ACADVL, ASGR1, 12 more genes
    nsv6591119inversion1nstd223human GRCh38 chr17: 5,860,086-7,699,509 , GRCh37.p13 chr17: 5,763,406-7,602,827 RPL23AP73, MIR195, 90 more genes
    nsv6589878inversion1nstd223human GRCh38 chr17: 1,213,690-8,318,220 , GRCh37.p13 chr17: 1,116,984-8,221,538 ASGR1, KIF1C-AS1, 321 more genes
    nsv6513639copy number variation1nstd223human GRCh38 chr17: 7,247,678-7,266,015 , GRCh37.p13 chr17: 7,150,997-7,169,334 CTDNEP1, CLDN7, 1 more genes
    nsv6504159copy number variation1nstd223human GRCh38 chr17: 7,248,176-7,255,968 , GRCh37.p13 chr17: 7,151,495-7,159,287 ELP5, CTDNEP1
    nsv6314103copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,020,054-8,086,290 , GRCh38.p12 chr17: 7,116,735-8,182,972 RPL7AP64, TNK1, 87 more genes
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