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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112755copy number variation1nstd102humanPathogenic GRCh37 chr12: 65,251,705-75,263,379 , GRCh38.p12 chr12: 64,857,925-74,869,599 LINC02421, TBC1D15, 144 more genes
    nsv5936094copy number variation1nstd209human GRCh38 chr12: 69,584,722-69,584,772 , GRCh37.p13 chr12: 69,978,502-69,978,552 CCT2, MIR3913-2, 1 more genes
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv5032581inversion1nstd200human GRCh38 chr12: 67,763,754-90,678,993 , GRCh37.p13 chr12: 68,157,534-91,072,770 , LOC105369886, 255 more genes
    nsv4888823inversion1nstd200human GRCh37 chr12: 68,157,543-91,072,771 , GRCh38.p12 chr12: 67,763,763-90,678,994 , BEST3, 255 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4729265copy number variation1nstd102humanPathogenic GRCh37 chr12: 68,572,386-70,833,868 , GRCh38.p12 chr12: 68,178,606-70,440,088 LINC02384, LOC101928002, 47 more genes
    nsv4610420copy number variation1nstd183human GRCh37 chr12: 69,991,448-69,991,745 , GRCh38.p12 chr12: 69,597,668-69,597,965 CCT2
    nsv4603586copy number variation1nstd183human GRCh37 chr12: 69,991,618-69,992,327 , GRCh38.p12 chr12: 69,597,838-69,598,547 CCT2
    nsv4345788sequence alteration1nstd166human GRCh37.p13 chr12: 59,785,153-101,478,055 , GRCh38.p12 chr12: 59,391,372-101,084,277 , APAF1, 538 more genes
    nsv4324772inversion1nstd166human GRCh37.p13 chr12: 27,368,635-91,765,744 , GRCh38.p12 chr12: 27,215,702-91,371,967 , ATP2B1, 1101 more genes
    nsv4209212copy number variation1nstd166human GRCh37.p13 chr12: 69,927,000-69,996,000 , GRCh38.p12 chr12: 69,533,220-69,602,220 CCT2, FRS2, 2 more genes
    nsv3918556copy number variation1nstd102humanLikely pathogenic NCBI36 chr12: 66,691,464-74,063,101 , GRCh37 chr12: 68,405,197-75,776,834 , GRCh38 chr12: 68,011,417-75,383,054 CPM, IFNG, 97 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
    nsv3911433copy number variation1nstd102humanPathogenic NCBI36 chr12: 64,125,223-69,706,384 , GRCh38 chr12: 65,445,176-71,026,337 , GRCh37 chr12: 65,838,956-71,420,117 SLC35E3, CCT2, 100 more genes
    nsv3909078copy number variation1nstd102humanBenign GRCh37 chr12: 69,887,817-70,022,135 , GRCh38.p12 chr12: 69,494,037-69,628,355 CCT2, LRRC10, 5 more genes
    nsv3905447copy number variation2nstd102humanPathogenic GRCh37 chr12: 173,787-133,777,902 , GRCh38.p12 chr12: 64,621-133,201,316 , LOH12CR2, 2452 more genes
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