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Items: 1 to 20 of 315

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7071535inversion1nstd229human GRCh38 chr9: 124,246,999-128,875,010 , GRCh37.p13 chr9: 127,009,278-131,637,289 PTGES2-AS1, STXBP1, 130 more genes
    nsv7060210inversion1nstd229human GRCh38 chr9: 128,073,407-128,102,224 , GRCh37.p13 chr9: 130,835,686-130,864,503 SLC25A25
    nsv6875827copy number variation1nstd229human GRCh38 chr9: 128,071,964-128,079,785 , GRCh37.p13 chr9: 130,834,243-130,842,064 SLC25A25
    nsv6873890copy number variation1nstd229human GRCh38 chr9: 128,107,212-128,110,600 , GRCh37.p13 chr9: 130,869,491-130,872,879 SLC25A25-AS1, SLC25A25
    nsv6872162copy number variation1nstd229human GRCh38 chr9: 127,958,825-128,098,837 , GRCh37.p13 chr9: 130,721,104-130,861,116 EEIG1, NAIF1, 1 more genes
    nsv6872014copy number variation1nstd229human GRCh38 chr9: 128,088,301-128,092,000 , GRCh37.p13 chr9: 130,850,580-130,854,279 SLC25A25
    nsv6869345copy number variation1nstd229human GRCh38 chr9: 127,951,402-128,083,324 , GRCh37.p13 chr9: 130,713,681-130,845,603 NAIF1, SLC25A25, 1 more genes
    nsv6867871copy number variation1nstd229human GRCh38 chr9: 128,076,501-128,086,400 , GRCh37.p13 chr9: 130,838,780-130,848,679 SLC25A25
    nsv6867331copy number variation1nstd229human GRCh38 chr9: 128,089,501-128,093,000 , GRCh37.p13 chr9: 130,851,780-130,855,279 SLC25A25
    nsv6866451copy number variation1nstd229human GRCh38 chr9: 128,076,538-128,086,374 , GRCh37.p13 chr9: 130,838,817-130,848,653 SLC25A25
    nsv6865628copy number variation1nstd229human GRCh38 chr9: 128,071,277-128,071,441 , GRCh37.p13 chr9: 130,833,556-130,833,720 SLC25A25
    nsv6862375copy number variation1nstd229human GRCh38 chr9: 128,081,134-128,081,338 , GRCh37.p13 chr9: 130,843,413-130,843,617 SLC25A25
    nsv6860927copy number variation1nstd229human GRCh38 chr9: 128,097,967-128,103,165 , GRCh37.p13 chr9: 130,860,246-130,865,444 SLC25A25
    nsv6860181copy number variation1nstd229human GRCh38 chr9: 128,058,001-128,071,700 , GRCh37.p13 chr9: 130,820,280-130,833,979 SLC25A25, NAIF1
    nsv6858409copy number variation1nstd229human GRCh38 chr9: 127,769,112-128,669,700 , GRCh37.p13 chr9: 130,531,391-131,431,979 BBLN, SH2D3C, 47 more genes
    nsv6858157copy number variation1nstd229human GRCh38 chr9: 128,079,047-128,161,482 , GRCh37.p13 chr9: 130,841,326-130,923,761 BBLN, PTGES2, 4 more genes
    nsv6634454copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-131,603,223 , GRCh38.p12 chr9: 203,861-128,840,944 HNRNPA1P41, GAS1RR, 1868 more genes
    nsv6633343copy number variation1nstd224human GRCh37 chr9: 130,778,514-130,851,573 , GRCh38.p12 chr9: 128,016,235-128,089,294 SLC25A25, NAIF1
    nsv6453506copy number variation1nstd223human GRCh38 chr9: 128,083,754-128,086,565 , GRCh37.p13 chr9: 130,846,033-130,848,844 SLC25A25
    nsv6447802copy number variation1nstd223human GRCh38 chr9: 128,079,801-128,081,700 , GRCh37.p13 chr9: 130,842,080-130,843,979 SLC25A25
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