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Items: 1 to 20 of 46

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3902105copy number variation1nstd102humanUncertain significance GRCh37 chr9: 131,622,711-131,689,418 , GRCh38.p12 chr9: 128,860,432-128,927,139 KYAT1, PHYHD1, 2 more genes
    nsv3899776copy number variation1nstd102humanPathogenic GRCh37 chr9: 129,370,440-133,866,894 , GRCh38.p12 chr9: 126,608,161-130,991,507 KYAT1, FNBP1, 136 more genes
    nsv3917587copy number variation1nstd102humanPathogenic NCBI36 chr9: 127,795,683-131,484,475 , GRCh38 chr9: 125,993,583-129,682,375 , GRCh37 chr9: 128,755,862-132,444,654 KYAT1, DYNC2I2, 115 more genes
    nsv3918361copy number variation1nstd102humanPathogenic NCBI36 chr9: 129,676,681-132,287,019 , GRCh38 chr9: 127,874,581-130,421,811 , GRCh37 chr9: 130,636,860-133,297,198 KYAT1, GOLGA2, 89 more genes
    nsv3903209copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,390,139-132,760,275 , GRCh38.p12 chr9: 127,627,860-129,997,996 KYAT1, PTRH1, 99 more genes
    nsv3909918copy number variation1nstd102humanPathogenic NCBI36 chr9: 129,933,505-131,594,414 , GRCh37.p13 chr9: 130,893,684-132,554,593 , GRCh38.p12 chr9: 128,131,405-129,792,314 KYAT1, C9orf50, 65 more genes
    nsv4675731copy number variation1nstd102humanPathogenic GRCh37 chr9: 130,957,344-132,310,210 , GRCh38.p12 chr9: 128,195,065-129,547,931 KYAT1, PTPA, 55 more genes
    nsv3914825copy number variation1nstd102humanPathogenic NCBI36 chr9: 129,873,497-130,897,002 , GRCh37.p13 chr9: 130,833,676-131,857,181 , GRCh38.p12 chr9: 128,071,397-129,094,902 KYAT1, RNU7-171P, 49 more genes
    nsv3924593copy number variation1nstd102humanPathogenic NCBI36 chr9: 130,038,447-130,714,167 , GRCh38 chr9: 128,236,347-128,912,067 , GRCh37 chr9: 130,998,626-131,674,346 KYAT1, LRRC8A, 34 more genes
    nsv3912247copy number variation1nstd102humanPathogenic NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981 KYAT1, ALOX15P2, 2184 more genes
    nsv3890420copy number variation1nstd102humanPathogenic GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797 KYAT1, TBC1D13, 2183 more genes
    nsv3905118copy number variation1nstd102humanPathogenic GRCh37 chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645 KYAT1, MIR219A2, 2183 more genes
    nsv3891842copy number variation1nstd102humanPathogenic GRCh37 chr9: 10,590-141,107,672 , GRCh38.p12 chr9: 10,590-138,217,222 KYAT1, OR13C1P, 2183 more genes
    nsv3895453copy number variation1nstd102humanPathogenic GRCh37 chr9: 46,587-141,066,491 , GRCh38.p12 chr9: 46,587-138,172,039 KYAT1, RPL19P15, 2176 more genes
    nsv3900967copy number variation1nstd102humanPathogenic GRCh37 chr9: 163,131-141,122,114 , GRCh38.p12 chr9: 163,131-138,231,664 KYAT1, BANCR, 2173 more genes
    nsv3907479copy number variation1nstd102humanPathogenic GRCh37 chr9: 62,525-141,006,407 , GRCh38.p12 chr9: 62,525-138,111,955 KYAT1, OR2AM1P, 2174 more genes
    nsv3922684copy number variation2nstd102humanPathogenic NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897 KYAT1, TDRD7, 2170 more genes
    nsv3919257copy number variation1nstd102humanPathogenic GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718 KYAT1, LOC107987031, 2169 more genes
    nsv3915973copy number variation2nstd102humanPathogenic GRCh38 chr9: 193,412-138,159,073 , GRCh37 chr9: 68,420,641-141,053,525 , NCBI36 chr9: 67,910,461-140,173,346 KYAT1, CTNNAL1, 2170 more genes
    nsv3911025copy number variation1nstd102humanPathogenic GRCh38 chr9: 193,412-138,124,524 , NCBI36 chr9: 194,090-140,138,797 , GRCh37 chr9: 204,090-141,018,976 KYAT1, RORB-AS1, 2168 more genes
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