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Items: 1 to 20 of 160

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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
    nsv6996852copy number variation1nstd229human GRCh38 chr17: 7,378,072-7,428,411 , GRCh37.p13 chr17: 7,281,391-7,331,730 PLSCR3, NLGN2, 6 more genes
    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
    nsv6994380copy number variation1nstd229human GRCh38 chr17: 7,392,901-7,394,900 , GRCh37.p13 chr17: 7,296,220-7,298,219 PLSCR3, TMEM256-PLSCR3
    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
    nsv6978572copy number variation1nstd229human GRCh38 chr17: 7,376,671-7,416,152 , GRCh37.p13 chr17: 7,279,990-7,319,471 TNK1, PLSCR3, 3 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
    nsv6507708copy number variation1nstd223human GRCh38 chr17: 7,393,833-7,396,795 , GRCh37.p13 chr17: 7,297,152-7,300,114 TMEM256-PLSCR3, PLSCR3
    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
    nsv6145348copy number variation1nstd206human GRCh38 chr17: 7,391,111-7,399,111 , GRCh37.p13 chr17: 7,294,430-7,302,430 TMEM256-PLSCR3, PLSCR3
    nsv6133424copy number variation2nstd213human GRCh37 chr17: 7,240,000-7,460,001 , GRCh38.p12 chr17: 7,336,681-7,556,684 , GRCh38.p12 chr17|NW_016107299.1: 1-154,723 CHRNB1, FGF11, 18 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
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