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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5495795copy number variation1nstd206human GRCh38 chr12: 128,629,846-129,247,751 , GRCh37.p13 chr12: 129,114,391-129,732,296 AK3P6, TMEM132D-AS2, 9 more genes
    nsv4993868copy number variation1nstd200human GRCh38 chr12: 128,791,180-129,272,727 , GRCh37.p13 chr12: 129,275,725-129,757,272 TMEM132D, AK3P6, 8 more genes
    nsv4830903copy number variation1nstd200human GRCh37 chr12: 129,275,725-129,757,272 , GRCh38.p12 chr12: 128,791,180-129,272,727 NLRP9P1, TMEM132D, 8 more genes
    nsv4675314copy number variation1nstd102humanUncertain significance GRCh37 chr12: 129,014,884-129,818,338 , GRCh38.p12 chr12: 128,530,339-129,333,793 TMEM132C, LOC100128276, 9 more genes
    nsv4456888copy number variation1nstd102humanUncertain significance GRCh37 chr12: 126,470,636-133,777,902 , GRCh38.p12 chr12: 125,986,090-133,201,316 LINC02347, LOC107987176, 145 more genes
    nsv4455689copy number variation1nstd102humanUncertain significance GRCh37 chr12: 129,299,049-129,628,826 , GRCh38.p12 chr12: 128,814,504-129,144,281 TMEM132D-AS1, GLT1D1, 6 more genes
    nsv4455426copy number variation1nstd102humanUncertain significance GRCh37 chr12: 128,503,810-130,456,374 , GRCh38.p12 chr12: 128,019,265-129,971,829 LINC02369, LOC105370074, 17 more genes
    nsv4349911copy number variation1nstd102humanPathogenic GRCh37 chr12: 125,451,405-133,810,935 , GRCh38.p12 chr12: 124,966,859-133,234,349 LOC107987177, GOLGA3, 159 more genes
    nsv4218279copy number variation1nstd166human GRCh37.p13 chr12: 129,530,410-129,637,213 , GRCh38.p12 chr12: 129,045,865-129,152,668 TMEM132D-AS1, TMEM132D
    nsv3961067copy number variation1nstd168human GRCh38 chr12: 129,078,390-129,160,006 , GRCh37.p13 chr12: 129,562,935-129,644,551 TMEM132D-AS1, TMEM132D
    nsv3924220copy number variation1nstd102humanPathogenic GRCh38 chr12: 115,131,583-133,166,920 , NCBI36 chr12: 114,053,771-132,253,579 , GRCh37 chr12: 115,569,388-133,743,506 LOC105370080, LINC02985, 376 more genes
    nsv3923347copy number variation1nstd102humanPathogenic NCBI36 chr12: 119,619,858-132,289,149 , GRCh37 chr12: 121,135,475-133,779,076 , GRCh38 chr12: 120,697,672-133,202,490 LOC105370044, RNU6-1017P, 273 more genes
    nsv3923155copy number variation1nstd102humanUncertain significance GRCh37 chr12: 128,385,044-130,262,839 , NCBI36 chr12: 126,950,997-128,828,792 , GRCh38 chr12: 127,900,499-129,778,294 MIR3612, AK3P6, 18 more genes
    nsv3921145copy number variation1nstd102humanPathogenic GRCh37 chr12: 123,929,305-133,767,986 , GRCh38 chr12: 123,444,758-133,191,400 , NCBI36 chr12: 122,495,258-132,278,059 ZNF268, PTP4A1P2, 193 more genes
    nsv3920565copy number variation1nstd102humanUncertain significance NCBI36 chr12: 127,537,816-128,376,317 , GRCh38 chr12: 128,487,318-129,325,819 , GRCh37 chr12: 128,971,863-129,810,364 TRI-AAT11-1, AK3P6, 9 more genes
    nsv3920557copy number variation1nstd102humanPathogenic GRCh37 chr12: 118,603,264-133,758,908 , GRCh38 chr12: 118,165,459-133,182,322 , NCBI36 chr12: 117,087,647-132,268,981 TMED2, GCN1, 339 more genes
    nsv3920031copy number variation1nstd102humanUncertain significance GRCh38 chr12: 128,510,404-129,187,569 , GRCh37 chr12: 128,994,949-129,672,114 , NCBI36 chr12: 127,560,902-128,238,067 TMEM132D, TMEM132C, 7 more genes
    nsv3915906copy number variation1nstd102humanPathogenic GRCh38 chr12: 126,403,612-133,166,920 , GRCh37 chr12: 126,888,158-133,743,506 , NCBI36 chr12: 125,454,111-132,253,579 FBRSL1, P2RX2, 135 more genes
    nsv3914999copy number variation1nstd102humanPathogenic NCBI36 chr12: 122,035,702-129,765,072 , GRCh38 chr12: 122,985,202-130,714,574 , GRCh37 chr12: 123,469,749-131,199,119 LINC00944, ATP6V0A2, 132 more genes
    nsv3914194copy number variation1nstd102humanPathogenic NCBI36 chr12: 100,698-132,283,466 , GRCh37 chr12: 282,465-133,773,393 , GRCh38 chr12: 121,271-133,196,807 , BTG1P1, 2451 more genes
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