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Items: 1 to 20 of 38

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3896498copy number variation1nstd102humanUncertain significance GRCh37 chr9: 129,416,212-129,644,627 , GRCh38.p12 chr9: 126,653,933-126,882,348 ZBTB34, LOC107987129, 2 more genes
    nsv6637981copy number variation1nstd102humanPathogenic GRCh37 chr9: 124,018,736-129,995,568 , GRCh38.p12 chr9: 121,256,458-127,233,289 ZBTB34, PBX3-DT, 119 more genes
    nsv3899776copy number variation1nstd102humanPathogenic GRCh37 chr9: 129,370,440-133,866,894 , GRCh38.p12 chr9: 126,608,161-130,991,507 ZBTB34, 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 ZBTB34, DYNC2I2, 115 more genes
    nsv3924370copy number variation1nstd102humanPathogenic NCBI36 chr9: 126,857,965-130,440,046 , GRCh38 chr9: 125,055,865-128,637,946 , GRCh37 chr9: 127,818,144-131,400,225 ZBTB34, MVB12B, 97 more genes
    nsv4768372copy number variation1nstd102humanPathogenic GRCh37 chr9: 128,512,347-130,702,572 , GRCh38.p12 chr9: 125,750,068-127,940,293 ZBTB34, LOC105379841, 47 more genes
    nsv3897949copy number variation1nstd102humanPathogenic GRCh37 chr9: 129,079,208-130,851,795 , GRCh38.p12 chr9: 126,316,929-128,089,516 ZBTB34, EEIG1, 44 more genes
    nsv3921944copy number variation1nstd102humanPathogenic GRCh38 chr9: 126,081,595-127,781,685 , NCBI36 chr9: 127,883,695-129,583,785 , GRCh37 chr9: 128,843,874-130,543,964 ZBTB34, LOC101929116, 30 more genes
    nsv5564479copy number variation2nstd102humanPathogenic, Uncertain significance GRCh37 chr9: 129,376,729-131,016,993 , GRCh38.p12 chr9: 126,614,450-128,254,714 ZBTB34, PIP5KL1, 50 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 ZBTB34, ALOX15P2, 2184 more genes
    nsv3890420copy number variation1nstd102humanPathogenic GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797 ZBTB34, TBC1D13, 2183 more genes
    nsv3905118copy number variation1nstd102humanPathogenic GRCh37 chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645 ZBTB34, MIR219A2, 2183 more genes
    nsv3891842copy number variation1nstd102humanPathogenic GRCh37 chr9: 10,590-141,107,672 , GRCh38.p12 chr9: 10,590-138,217,222 ZBTB34, OR13C1P, 2183 more genes
    nsv3895453copy number variation1nstd102humanPathogenic GRCh37 chr9: 46,587-141,066,491 , GRCh38.p12 chr9: 46,587-138,172,039 ZBTB34, RPL19P15, 2176 more genes
    nsv3900967copy number variation1nstd102humanPathogenic GRCh37 chr9: 163,131-141,122,114 , GRCh38.p12 chr9: 163,131-138,231,664 ZBTB34, BANCR, 2173 more genes
    nsv3907479copy number variation1nstd102humanPathogenic GRCh37 chr9: 62,525-141,006,407 , GRCh38.p12 chr9: 62,525-138,111,955 ZBTB34, 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 ZBTB34, 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 ZBTB34, 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 ZBTB34, 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 ZBTB34, RORB-AS1, 2168 more genes
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