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Items: 1 to 20 of 251

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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
    nsv7098743copy number variation1nstd102humanUncertain significance GRCh37 chr17: 422,368-2,585,096 , GRCh38.p12 chr17: 519,128-2,681,802 PAFAH1B1, RN7SL33P, 65 more genes
    nsv7077625inversion1nstd229human GRCh38 chr17: 626,377-3,112,687 , GRCh37.p13 chr17: 529,617-3,015,981 MIR3183, YWHAE, 75 more genes
    nsv7075634inversion1nstd229human GRCh38 chr17: 1,370,296-2,529,284 , GRCh37.p13 chr17: 1,273,590-2,432,578 MCUR1P1, CRK, 42 more genes
    nsv7074630inversion1nstd229human GRCh38 chr17: 1,926,290-3,643,131 , GRCh37.p13 chr17: 1,829,584-3,546,425 SAMD11P1, LOC100288728, 61 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
    nsv7072232inversion1nstd229human GRCh38 chr17: 1,370,504-2,529,584 , GRCh37.p13 chr17: 1,273,798-2,432,878 MNT, SMG6, 42 more genes
    nsv7064412inversion1nstd229human GRCh38 chr17: 1,889,974-2,404,651 , GRCh37.p13 chr17: 1,793,268-2,307,945 SRR, RTN4RL1, 20 more genes
    nsv7062153inversion1nstd229human GRCh38 chr17: 1,536,285-2,124,548 , GRCh37.p13 chr17: 1,439,579-2,027,842 MIR132, SLC43A2, 23 more genes
    nsv7061251inversion1nstd229human GRCh38 chr17: 1,526,162-2,202,888 , GRCh37.p13 chr17: 1,429,456-2,106,182 LOC107984988, RILP, 25 more genes
    nsv6995909copy number variation1nstd229human GRCh38 chr17: 1,989,316-2,154,356 , GRCh37.p13 chr17: 1,892,610-2,057,650 MIR212, RTN4RL1, 9 more genes
    nsv6987167copy number variation1nstd229human GRCh38 chr17: 2,036,501-2,082,400 , GRCh37.p13 chr17: 1,939,795-1,985,694 MIR132, DPH1, 5 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
    nsv6637325copy number variation1nstd102humanPathogenic GRCh37 chr17: 1,095,592-3,484,368 , GRCh38.p12 chr17: 1,192,298-3,581,074 SLC43A2, LOC105371592, 81 more genes
    nsv6637292copy number variation1nstd102humanUncertain significance GRCh37 chr17: 1,377,247-2,455,613 , GRCh38.p12 chr17: 1,473,953-2,552,319 RPA1, TLCD2, 40 more genes
    nsv6624054copy number variation2nstd224human GRCh37 chr17: 1,897,820-2,050,166 , GRCh38.p12 chr17: 1,994,526-2,146,872 OVCA2, SMG6, 9 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
    nsv6499904copy number variation1nstd223human GRCh38 chr17: 2,062,792-2,063,662 , GRCh37.p13 chr17: 1,966,086-1,966,956 HIC1, SMG6
    nsv6203632copy number variation1nstd214human GRCh38 chr17: 2,059,082-2,059,143 , GRCh37.p13 chr17: 1,962,376-1,962,437 SMG6, HIC1
    nsv5554086sequence alteration1nstd206human GRCh38 chr17: 2,002,441-2,408,835 , GRCh37.p13 chr17: 1,905,735-2,312,129 SMG6, TSR1, 20 more genes
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