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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5929605copy number variation1nstd209human GRCh38 chr17: 8,496,427-8,496,595 , GRCh37.p13 chr17: 8,399,745-8,399,913 , MYH10
    nsv5929452copy number variation1nstd209human GRCh38 chr17: 6,412,133-13,962,466 , GRCh37.p13 chr17: 6,315,453-13,865,783 , PIK3R5-DT, 226 more genes
    nsv5015796copy number variation1nstd200human GRCh38 chr17: 8,495,680-8,497,018 , GRCh37.p13 chr17: 8,398,998-8,400,336 , MYH10
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv3917059copy number variation1nstd102humanPathogenic GRCh37 chr17: 45,835-12,247,218 , NCBI36 chr17: 11,807-12,187,943 , GRCh38 chr17: 162,016-12,343,901 PSMB6, RNU6-1065P, 409 more genes
    nsv3915354copy number variation1nstd102humanPathogenic GRCh38 chr17: 150,732-14,764,202 , NCBI36 chr17: 525-14,608,244 , GRCh37 chr17: 525-14,667,519 KIF1C-AS1, TMEM107, 433 more genes
    nsv3911050copy number variation1nstd102humanPathogenic GRCh38 chr17: 5,732,953-12,095,349 , GRCh37 chr17: 5,636,273-11,998,666 , NCBI36 chr17: 5,576,997-11,939,391 C17orf49, SPEM1, 209 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 MIR21, LOC105371899, 2366 more genes
    nsv3904771copy number variation1nstd102humanPathogenic GRCh37 chr17: 525-11,186,432 , GRCh38.p12 chr17: 150,732-11,283,115 SLC2A4, CCDC92B, 401 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 MIR3185, YWHAEP6, 2366 more genes
    nsv3902311copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,929,776-9,995,862 , GRCh38.p12 chr17: 8,026,458-10,092,545 RCVRN, TRQ-CTG1-5, 74 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 P4HB, LOC105371808, 2366 more genes
    nsv3899694copy number variation1nstd102humanUncertain significance GRCh37 chr17: 7,431,013-9,868,179 , GRCh38.p12 chr17: 7,527,696-9,964,862 VAMP2, RPL19P18, 109 more genes
    nsv3898050copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,241,916-8,692,213 , GRCh38.p12 chr17: 7,338,597-8,788,895 NDEL1, SENP3-EIF4A1, 108 more genes
    nsv3897625copy number variation1nstd102humanPathogenic GRCh37 chr17: 525-15,027,737 , GRCh38.p12 chr17: 150,732-15,124,420 GP1BA, POLR2A, 439 more genes
    nsv3890702copy number variation1nstd102humanUncertain significance GRCh37 chr17: 8,219,814-8,676,240 , GRCh38.p12 chr17: 8,316,496-8,772,922 LOC105371530, RNU7-43P, 17 more genes
    nsv3143440copy number variation1nstd151human GRCh37 chr17: 8,092,382-8,424,608 , GRCh38.p12 chr17: 8,189,064-8,521,290 , TRP-CGG1-3, 24 more genes
    nsv3141304copy number variation1nstd151human GRCh37 chr17: 8,092,382-8,413,272 , GRCh38.p12 chr17: 8,189,064-8,509,954 , BORCS6, 24 more genes
    esv4010477copy number variation1estd233human GRCh37 chr17: 8,213,000-8,585,000 , GRCh38.p12 chr17: 8,309,682-8,681,682 , MYH10, 13 more genes
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