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Items: 1 to 20 of 262

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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
    nsv7098192copy number variation1nstd102humanPathogenic GRCh37 chr9: 108,335,926-108,403,409 , GRCh38.p12 chr9: 105,573,645-105,641,128 FKTN
    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
    nsv7098047copy number variation1nstd102humanLikely pathogenic GRCh37 chr9: 108,377,539-108,377,708 , GRCh38.p12 chr9: 105,615,258-105,615,427 FKTN
    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
    nsv7097680copy number variation1nstd102humanUncertain significance GRCh37 chr9: 108,397,312-108,397,545 , GRCh38.p12 chr9: 105,635,031-105,635,264 FKTN
    nsv7097679copy number variation1nstd102humanPathogenic GRCh37 chr9: 108,377,549-108,382,383 , GRCh38.p12 chr9: 105,615,268-105,620,102 FKTN
    nsv7070627inversion1nstd229human GRCh38 chr9: 105,586,952-105,590,557 , GRCh37.p13 chr9: 108,349,233-108,352,838 FKTN
    nsv7064749inversion1nstd229human GRCh38 chr9: 105,592,513-105,599,517 , GRCh37.p13 chr9: 108,354,794-108,361,798 FKTN
    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
    nsv6870160copy number variation1nstd229human GRCh38 chr9: 105,561,190-105,561,539 , GRCh37.p13 chr9: 108,323,471-108,323,820 FKTN
    nsv6866379copy number variation1nstd229human GRCh38 chr9: 105,610,030-105,611,115 , GRCh37.p13 chr9: 108,372,311-108,373,396 FKTN
    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
    nsv6858749copy number variation1nstd229human GRCh38 chr9: 105,632,543-105,844,896 , GRCh37.p13 chr9: 108,394,824-108,607,177 LOC107987107, TMEM38B, 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
    nsv6564746inversion1nstd223human GRCh38 chr9: 105,603,697-105,604,949 , GRCh37.p13 chr9: 108,365,978-108,367,230 FKTN
    nsv6564558inversion1nstd223human GRCh38 chr9: 105,545,205-105,764,347 , GRCh37.p13 chr9: 108,307,486-108,526,628 FKTN, TAL2, 6 more genes
    nsv6454410copy number variation1nstd223human GRCh38 chr9: 105,577,701-105,579,000 , GRCh37.p13 chr9: 108,339,982-108,341,281 FKTN
    nsv6450403copy number variation1nstd223human GRCh38 chr9: 105,591,463-105,592,318 , GRCh37.p13 chr9: 108,353,744-108,354,599 FKTN
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