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Items: 1 to 20 of 190

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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
    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
    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
    nsv6996918copy number variation1nstd229human GRCh38 chr17: 7,170,791-7,181,273 , GRCh37.p13 chr17: 7,074,110-7,084,592 ASGR1
    nsv6985013copy number variation1nstd229human GRCh38 chr17: 7,163,209-7,191,501 , GRCh37.p13 chr17: 7,066,528-7,094,820 ASGR1, DLG4
    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
    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
    nsv6133245copy number variation1nstd213human GRCh37 chr17: 4,010,000-8,220,001 , GRCh38.p12 chr17: 4,106,706-8,316,683 ACADVL, ALOX12, 220 more genes
    nsv6133065copy number variation1nstd213human GRCh37 chr17: 4,530,000-8,270,001 , GRCh38.p12 chr17: 4,626,705-8,366,683 ACADVL, ALOX12, 206 more genes
    nsv6133064copy number variation1nstd213human GRCh37 chr17: 4,520,000-8,470,001 , GRCh38.p12 chr17: 4,616,705-8,566,683 ACADVL, ALOX12, 217 more genes
    nsv5929452copy number variation1nstd209human GRCh38 chr17: 6,412,133-13,962,466 , GRCh37.p13 chr17: 6,315,453-13,865,783 , PIK3R5-DT, 226 more genes
    nsv5673052copy number variation1nstd102humanPathogenic GRCh37 chr17: 6,589,506-7,128,436 , GRCh38.p12 chr17: 6,686,187-7,225,117 RPL23AP73, MIR195, 25 more genes
    nsv5381181copy number variation1nstd102humanUncertain significance GRCh37 chr17: 6,328,780-7,128,416 , GRCh38.p12 chr17: 6,425,460-7,225,097 RNA5SP435, RPL23AP73, 37 more genes
    nsv5290585copy number variation1nstd204human GRCh38.p13 chr17: 7,132,501-7,211,000 , GRCh37.p13 chr17: 7,035,820-7,114,319 ASGR1, LOC105371512, 2 more genes
    nsv5283638copy number variation1nstd204human GRCh38.p13 chr17: 6,923,801-7,855,300 , GRCh37.p13 chr17: 6,827,120-7,758,618 , TNFSF12, 74 more genes
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