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Items: 1 to 20 of 115

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096952copy number variation3nstd102humanUncertain significance GRCh37 chr3: 188,118,572-192,126,012 , GRCh38.p12 chr3: 188,400,784-192,408,223 P3H2, GMNC, 39 more genes
    nsv7096556copy number variation1nstd102humanUncertain significance GRCh37 chr3: 189,455,509-192,126,012 , GRCh38.p12 chr3: 189,737,720-192,408,223 LOC107986171, OSTN, 30 more genes
    nsv7042759inversion1nstd229human GRCh38 chr3: 189,828,250-189,831,838 , GRCh37.p13 chr3: 189,546,039-189,549,627 MIR944, TP63
    nsv7040429inversion1nstd229human GRCh38 chr3: 184,379,670-192,292,047 , GRCh37.p13 chr3: 184,097,458-192,009,836 LOC107986163, RPL34P10, 123 more genes
    nsv6725952copy number variation1nstd229human GRCh38 chr3: 189,699,027-190,504,616 , GRCh37.p13 chr3: 189,416,816-190,222,405 CLDN16, P3H2, 8 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6315437copy number variation1nstd102humanPathogenic GRCh37 chr3: 183,498,520-197,851,986 , GRCh38.p12 chr3: 183,780,732-198,125,115 LOC105374291, GP5, 315 more genes
    nsv6313869copy number variation1nstd102humanUncertain significance GRCh37 chr3: 189,402,113-189,899,616 , GRCh38.p12 chr3: 189,684,324-190,181,827 TP63, NMNAT1P3, 5 more genes
    nsv6311971copy number variation1nstd102humanUncertain significance GRCh37 chr3: 189,349,285-189,612,311 , GRCh38.p12 chr3: 189,631,496-189,894,522 MIR944, TP63
    nsv6134833copy number variation1nstd213human GRCh37 chr3: 186,910,000-193,810,001 , GRCh38.p12 chr3: 187,192,212-194,092,212 BCL6, LPP, 85 more genes
    nsv5453639copy number variation1nstd206human GRCh38 chr3: 163,047,000-198,226,000 , GRCh37.p13 chr3: 162,764,788-197,952,871 , MIR922, 587 more genes
    nsv4707895copy number variation1nstd195human GRCh37 chr3: 189,407,151-189,831,551 , GRCh38.p12 chr3: 189,689,362-190,113,762 TP63, P3H2, 2 more genes
    nsv4674680copy number variation1nstd102humanPathogenic GRCh37 chr3: 169,617,690-190,593,854 , GRCh38.p12 chr3: 169,899,902-190,876,065 RNU6-1120P, LOC105374262, 323 more genes
    nsv4561014sequence alteration1nstd166human GRCh37.p13 chr3: 189,545,971-189,549,722 , GRCh38.p12 chr3: 189,828,182-189,831,933 TP63, MIR944
    nsv4436392copy number variation1nstd102humanPathogenic GRCh37 chr3: 188,386,566-197,838,262 , GRCh38.p12 chr3: 188,668,778-198,111,391 PPP1R2, GCNT1P3, 194 more genes
    nsv4366973copy number variation1nstd173human GRCh37 chr3: 189,445,224-189,561,865 , GRCh38.p12 chr3: 189,727,435-189,844,076 TP63, MIR944
    nsv4327395inversion1nstd166human GRCh37.p13 chr3: 126,265,569-194,265,571 , GRCh38.p12 chr3: 126,546,726-194,544,842 , ACTG1P1, 1039 more genes
    nsv4102304copy number variation1nstd166human GRCh37.p13 chr3: 189,416,756-190,222,423 , GRCh38.p12 chr3: 189,698,967-190,504,634 TMEM207, RNU6-1109P, 8 more genes
    nsv3923340copy number variation1nstd102humanPathogenic GRCh38 chr3: 187,446,231-190,839,052 , GRCh37 chr3: 187,164,019-190,556,841 , NCBI36 chr3: 188,646,713-192,039,535 ENOPH1P1, LINC01991, 36 more genes
    nsv3922385copy number variation1nstd102humanPathogenic NCBI36 chr3: 177,369,007-199,329,651 , GRCh37 chr3: 175,886,313-197,845,254 , GRCh38 chr3: 176,168,525-198,118,383 LINC02053, RTP4, 414 more genes
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