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Items: 1 to 20 of 153

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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
    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
    nsv7095365copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,571,752-8,285,628 , GRCh38.p12 chr17: 7,668,434-8,382,310 TRK-TTT3-5, WRAP53, 59 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
    nsv7063892inversion1nstd229human GRCh38 chr17: 7,895,855-10,701,597 , GRCh37.p13 chr17: 7,799,173-10,604,914 CHD3, MYH4, 92 more genes
    nsv6995236copy number variation1nstd229human GRCh38 chr17: 8,195,497-8,202,964 , GRCh37.p13 chr17: 8,098,815-8,106,282 AURKB
    nsv6994999copy number variation1nstd229human GRCh38 chr17: 8,210,943-8,219,384 , GRCh37.p13 chr17: 8,114,261-8,122,702 TRW-CCA1-1, LINC00324, 1 more genes
    nsv6983819copy number variation1nstd229human GRCh38 chr17: 8,177,208-8,206,738 , GRCh37.p13 chr17: 8,080,526-8,110,056 BORCS6, TRS-GCT4-3, 6 more genes
    nsv6982823copy number variation1nstd229human GRCh38 chr17: 8,148,126-8,376,847 , GRCh37.p13 chr17: 8,051,444-8,280,165 TRW-CCA1-1, TRG-TCC3-1, 27 more genes
    nsv6982091copy number variation1nstd229human GRCh38 chr17: 8,180,039-8,224,370 , GRCh37.p13 chr17: 8,083,357-8,127,688 AURKB, MIR4521, 13 more genes
    nsv6981148copy number variation1nstd229human GRCh38 chr17: 8,113,981-8,206,922 , GRCh37.p13 chr17: 8,017,299-8,110,240 VAMP2, LOC105371520, 20 more genes
    nsv6624129copy number variation1nstd224human GRCh37 chr17: 8,109,861-8,215,679 , GRCh38.p12 chr17: 8,206,543-8,312,361 AURKB, RANGRF, 12 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
    nsv6513806copy number variation1nstd223human GRCh38 chr17: 7,990,455-8,357,154 , GRCh37.p13 chr17: 7,893,773-8,260,472 TRR-TCT2-1, TRP-CGG1-3, 41 more genes
    nsv6512711copy number variation1nstd223human GRCh38 chr17: 8,195,496-8,202,963 , GRCh37.p13 chr17: 8,098,814-8,106,281 AURKB
    nsv6505053copy number variation1nstd223human GRCh38 chr17: 8,203,255-8,213,082 , GRCh37.p13 chr17: 8,106,573-8,116,400 AURKB
    nsv6314215copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,593,552-8,225,803 , GRCh38.p12 chr17: 7,690,234-8,322,485 GUCY2D, LOC105371520, 54 more genes
    nsv6310334copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,571,752-8,135,555 , GRCh38.p12 chr17: 7,668,434-8,232,237 TRAPPC1, MIR4314, 51 more genes
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