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Items: 1 to 20 of 191

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5297254copy number variation1nstd204human GRCh38.p13 chr17: 1,311,601-1,752,100 , GRCh37.p13 chr17: 1,214,895-1,655,394 RN7SL105P, SCARF1, 15 more genes
    nsv5283059copy number variation1nstd204human GRCh38.p13 chr17: 1,690,401-1,723,500 , GRCh37.p13 chr17: 1,593,695-1,626,794 MIR22HG, MIR22, 2 more genes
    nsv5023532copy number variation1nstd200human GRCh38 chr17: 1,537,111-1,929,680 , GRCh37.p13 chr17: 1,440,405-1,832,974 SLC43A2, PRPF8, 13 more genes
    nsv4769394copy number variation1nstd102humanUncertain significance GRCh37 chr17: 722,145-1,875,784 , GRCh38.p12 chr17: 818,905-1,972,490 SCARF1, WDR81, 31 more genes
    nsv4768381copy number variation1nstd102humanPathogenic GRCh37 chr17: 84,287-2,468,384 , GRCh38.p12 chr17: 234,496-2,565,090 GLOD4, RTN4RL1, 67 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4685767copy number variation1nstd102humanPathogenic GRCh38 chr17: 1,113,701-1,844,036 , GRCh37.p13 chr17: 1,016,941-1,747,330 WDR81, PITPNA-AS1, 24 more genes
    nsv4675624copy number variation1nstd102humanPathogenic GRCh37 chr17: 525-2,221,159 , GRCh38.p12 chr17: 150,732-2,317,865 HNRNPA1P16, RTN4RL1, 60 more genes
    nsv4675387copy number variation1nstd102humanPathogenic GRCh37 chr17: 1,009,449-1,722,313 , GRCh38.p12 chr17: 1,106,209-1,819,019 PITPNA-AS1, YWHAE, 23 more genes
    nsv4675180copy number variation1nstd102humanUncertain significance GRCh37 chr17: 1,310,685-1,690,452 , GRCh38.p12 chr17: 1,407,391-1,787,158 , GRCh38.p12 chr17|NT_187611.1: 1-196,688 MIR22HG, MIR22, 16 more genes
    nsv4675133copy number variation1nstd102humanPathogenic GRCh37 chr17: 1,204,863-1,751,418 , GRCh38.p12 chr17: 1,301,569-1,848,124 YWHAE, TLCD2, 18 more genes
    nsv4674912copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-5,627,408 , GRCh38.p12 chr17: 158,756-5,724,088 SRR, DBIL5P, 196 more genes
    nsv4457568copy number variation1nstd102humanPathogenic GRCh37 chr17: 1,501,331-2,832,123 , GRCh38.p12 chr17: 1,598,037-2,928,829 TSR1, LOC284009, 47 more genes
    nsv4431000copy number variation1nstd174human GRCh37 chr17: 1,545,902-1,617,029 , GRCh38.p12 chr17: 1,642,608-1,713,735 , GRCh38.p12 chr17|NT_187611.1: 72,636-143,763 SCARF1, PRPF8, 4 more genes
    nsv4368798copy number variation1nstd173human GRCh37 chr17: 1,485,295-2,355,965 , GRCh38.p12 chr17: 1,582,001-2,452,671 RPA1, MIR132, 35 more genes
    nsv4350781copy number variation1nstd102humanPathogenic GRCh37 chr17: 47,546-6,287,620 , GRCh38.p12 chr17: 197,755-6,384,300 SERPINF1, UBE2G1, 201 more genes
    nsv4237808copy number variation1nstd166human GRCh37.p13 chr17: 1,485,414-2,431,916 , GRCh38.p12 chr17: 1,582,120-2,528,622 TLCD2, RN7SL624P, 35 more genes
    nsv3923943copy number variation1nstd102humanPathogenic NCBI36 chr17: 84,287-2,235,556 , GRCh37 chr17: 396,627-2,288,806 , GRCh38 chr17: 234,496-2,385,512 INPP5K, VPS53, 64 more genes
    nsv3923881copy number variation1nstd102humanPathogenic NCBI36 chr17: 48,539-4,989,051 , GRCh37.p13 chr17: 48,539-5,048,327 , GRCh38.p12 chr17: 198,748-5,145,032 CAMKK1, MIR6776, 177 more genes
    nsv3923748copy number variation1nstd102humanPathogenic NCBI36 chr17: 6,333-2,151,032 , GRCh37.p13 chr17: 6,333-2,204,282 , GRCh38.p12 chr17: 156,542-2,300,988 DPH1, LOC105371486, 58 more genes
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