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Items: 1 to 20 of 268

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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
    nsv7098729copy number variation1nstd102humanPathogenic GRCh37 chr17: 422,368-1,945,151 , GRCh38.p12 chr17: 519,128-2,041,857 MYO1C, SERPINF1, 42 more genes
    nsv7095131copy number variation1nstd102humanPathogenic GRCh37 chr17: 1,478,898-1,642,177 , GRCh38.p12 chr17: 1,575,604-1,738,883 , GRCh38.p12 chr17|NT_187611.1: 5,632-168,923 SCARF1, PRPF8, 7 more genes
    nsv7094896copy number variation1nstd102humanUncertain significance GRCh37 chr17: 422,368-1,680,740 , GRCh38.p12 chr17: 519,128-1,777,446 SLC43A2, LOC105371480, 34 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
    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
    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
    nsv6997734copy number variation1nstd229human GRCh38 chr17: 1,591,835-1,684,780 , GRCh37.p13 chr17: 1,495,129-1,588,074 RILP, RN7SL105P, 3 more genes
    nsv6983949copy number variation1nstd229human GRCh38 chr17: 1,601,566-1,696,784 , GRCh37.p13 chr17: 1,504,860-1,600,078 SCARF1, RN7SL105P, 3 more genes
    nsv6981420copy number variation1nstd229human GRCh38 chr17: 1,598,301-1,603,600 , GRCh37.p13 chr17: 1,501,595-1,506,894 RN7SL105P, SLC43A2
    nsv6637505copy number variation1nstd102humanPathogenic GRCh37 chr17: 526-1,690,452 , GRCh38.p12 chr17: 150,733-1,787,158 RPS4XP17, LIAT1, 43 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
    nsv6624008copy number variation1nstd224human GRCh37 chr17: 1,444,702-1,731,230 , GRCh38.p12 chr17: 1,541,408-1,827,936 , GRCh38.p12 chr17|NT_187611.1: 1-196,688 SCARF1, WDR81, 11 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
    nsv6586367inversion1nstd223human GRCh38 chr17: 1,603,702-1,604,352 , GRCh37.p13 chr17: 1,506,996-1,507,646 SLC43A2, RN7SL105P
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