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Items: 1 to 20 of 238

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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
    nsv7145464copy number variation1nstd232human GRCh37.p13 chr17: 7,530,361-7,530,458 , GRCh38.p12 chr17: 7,627,043-7,627,140 SHBG, SAT2
    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
    nsv6997294copy number variation1nstd229human GRCh38 chr17: 7,632,580-7,671,102 , GRCh37.p13 chr17: 7,535,898-7,574,420 TP53, ATP1B2, 1 more genes
    nsv6994015copy number variation1nstd229human GRCh38 chr17: 7,616,785-7,617,333 , GRCh37.p13 chr17: 7,520,103-7,520,651 SHBG
    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
    nsv6979648copy number variation1nstd229human GRCh38 chr17: 7,629,033-7,629,356 , GRCh37.p13 chr17: 7,532,351-7,532,674 SHBG
    nsv6978829copy number variation1nstd229human GRCh38 chr17: 7,621,099-7,621,706 , GRCh37.p13 chr17: 7,524,417-7,525,024 TRUND-NNN6-1, SHBG
    nsv6637360copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,381,537-8,068,400 , GRCh38.p12 chr17: 7,478,218-8,165,082 LOC107985075, TRT-AGT5-1, 53 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
    nsv6586222inversion1nstd223human GRCh38 chr17: 7,622,039-7,623,005 , GRCh37.p13 chr17: 7,525,357-7,526,323 SHBG
    nsv6585334inversion1nstd223human GRCh38 chr17: 7,624,964-7,625,496 , GRCh37.p13 chr17: 7,528,282-7,528,814 SAT2, SHBG
    nsv6579059inversion1nstd223human GRCh38 chr17: 7,628,431-7,628,864 , GRCh37.p13 chr17: 7,531,749-7,532,182 SHBG
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