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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148263copy number variation1nstd102humanPathogenic GRCh38 chr9: 102,995,214-108,903,040 , GRCh37.p13 chr9: 105,757,496-111,665,320 ACTL7B, OR13C3, 88 more genes
    nsv7144431insertion1nstd232human GRCh37.p13 chr9: 108,510,477-108,510,477 , GRCh38.p12 chr9: 105,748,196-105,748,196 TMEM38B
    nsv7098751copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 108,484,903-108,538,893 , GRCh38.p12 chr9: 105,722,622-105,776,612 TMEM38B, DEPDC1P2
    nsv7098191copy number variation1nstd102humanUncertain significance GRCh37 chr9: 107,546,596-108,536,361 , GRCh38.p12 chr9: 104,784,315-105,774,080 TMEM38B, CT70, 14 more genes
    nsv7097919copy number variation1nstd102humanPathogenic GRCh37 chr9: 108,467,858-108,536,361 , GRCh38.p12 chr9: 105,705,577-105,774,080 TMEM38B, LOC107987107, 2 more genes
    nsv7097918copy number variation1nstd102humanPathogenic GRCh37 chr9: 108,456,942-108,536,361 , GRCh38.p12 chr9: 105,694,661-105,774,080 TMEM38B, LOC107987107, 2 more genes
    nsv7097917copy number variation1nstd102humanPathogenic GRCh37 chr9: 108,358,859-108,484,922 , GRCh38.p12 chr9: 105,596,578-105,722,641 FKTN, TAL2, 3 more genes
    nsv7075258inversion1nstd229human GRCh38 chr9: 105,659,939-106,272,714 , GRCh37.p13 chr9: 108,422,220-109,034,995 LOC107987107, TMEM38B, 6 more genes
    nsv7071806inversion1nstd229human GRCh38 chr9: 105,659,830-105,919,918 , GRCh37.p13 chr9: 108,422,111-108,682,199 DEPDC1P2, TAL2, 4 more genes
    nsv7062784inversion1nstd229human GRCh38 chr9: 105,247,017-105,897,262 , GRCh37.p13 chr9: 108,009,298-108,659,543 SLC44A1, RALGAPA1P1, 9 more genes
    nsv7058700inversion1nstd229human GRCh38 chr9: 105,563,937-105,790,249 , GRCh37.p13 chr9: 108,326,218-108,552,530 DEPDC1P2, LOC100421293, 4 more genes
    nsv6877608copy number variation1nstd229human GRCh38 chr9: 105,682,311-105,716,200 , GRCh37.p13 chr9: 108,444,592-108,478,481 TMEM38B, LOC100421293, 1 more genes
    nsv6874674copy number variation1nstd229human GRCh38 chr9: 105,708,262-105,713,113 , GRCh37.p13 chr9: 108,470,543-108,475,394 LOC100421293, LOC107987107, 1 more genes
    nsv6873944copy number variation1nstd229human GRCh38 chr9: 105,760,657-105,765,896 , GRCh37.p13 chr9: 108,522,938-108,528,177 TMEM38B, DEPDC1P2
    nsv6868057copy number variation1nstd229human GRCh38 chr9: 105,702,195-105,703,070 , GRCh37.p13 chr9: 108,464,476-108,465,351 TMEM38B
    nsv6867603copy number variation1nstd229human GRCh38 chr9: 105,730,101-105,767,500 , GRCh37.p13 chr9: 108,492,382-108,529,781 TMEM38B, DEPDC1P2
    nsv6865511copy number variation1nstd229human GRCh38 chr9: 105,694,435-105,715,860 , GRCh37.p13 chr9: 108,456,716-108,478,141 TMEM38B, LOC100421293, 1 more genes
    nsv6865426copy number variation1nstd229human GRCh38 chr9: 105,630,787-105,698,163 , GRCh37.p13 chr9: 108,393,068-108,460,444 TAL2, TMEM38B, 1 more genes
    nsv6865406copy number variation1nstd229human GRCh38 chr9: 105,698,720-105,722,887 , GRCh37.p13 chr9: 108,461,001-108,485,168 TMEM38B, LOC100421293, 1 more genes
    nsv6863610copy number variation1nstd229human GRCh38 chr9: 105,773,118-105,968,206 , GRCh37.p13 chr9: 108,535,399-108,730,487 LOC107987108, SLC25A6P5, 1 more genes
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