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Items: 1 to 20 of 225

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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
    nsv6996010copy number variation1nstd229human GRCh38 chr17: 2,398,142-2,400,008 , GRCh37.p13 chr17: 2,301,436-2,303,302 MNT
    nsv6984455copy number variation1nstd229human GRCh38 chr17: 2,134,094-2,519,893 , GRCh37.p13 chr17: 2,037,388-2,423,187 RN7SL624P, TSR1, 11 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
    nsv6982020copy number variation1nstd229human GRCh38 chr17: 2,392,901-2,396,300 , GRCh37.p13 chr17: 2,296,195-2,299,594 MNT
    nsv6978217copy number variation1nstd229human GRCh38 chr17: 2,107,110-2,808,938 , GRCh37.p13 chr17: 2,010,404-2,712,232 PAFAH1B1, SAMD11P1, 24 more genes
    nsv6637877copy number variation1nstd102humanPathogenic GRCh37 chr17: 2,161,424-2,825,460 , GRCh38.p12 chr17: 2,258,130-2,922,166 SRR, HNRNPA1P16, 21 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
    nsv6592364inversion1nstd223human GRCh38 chr17: 2,078,667-6,081,513 , GRCh37.p13 chr17: 1,981,961-5,984,833 MYBBP1A, CXCL16, 143 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
    nsv6506202copy number variation1nstd223human GRCh38 chr17: 2,392,601-2,393,000 , GRCh37.p13 chr17: 2,295,895-2,296,294 MNT
    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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