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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054823inversion1nstd229human GRCh38 chr6: 143,170,072-148,803,855 , GRCh37.p13 chr6: 143,491,209-149,124,991 FBXO30, C4orf46P4, 56 more genes
    nsv7053654inversion1nstd229human GRCh38 chr6: 143,517,092-147,615,699 , GRCh37.p13 chr6: 143,838,229-147,936,835 PHACTR2, LOC105378040, 37 more genes
    nsv6804779copy number variation1nstd229human GRCh38 chr6: 146,558,546-146,668,601 , GRCh37.p13 chr6: 146,879,682-146,989,737 ADGB-DT, ADGB
    nsv6804410copy number variation1nstd229human GRCh38 chr6: 146,523,401-146,610,000 , GRCh37.p13 chr6: 146,844,537-146,931,136 ADGB-DT, ADGB, 1 more genes
    nsv6800855copy number variation1nstd229human GRCh38 chr6: 146,490,912-146,607,905 , GRCh37.p13 chr6: 146,812,048-146,929,041 RAB32, ADGB-DT, 1 more genes
    nsv6798381copy number variation1nstd229human GRCh38 chr6: 146,249,035-146,800,727 , GRCh37.p13 chr6: 146,570,171-147,121,863 RAB32, KATNBL1P6, 5 more genes
    nsv6313499copy number variation1nstd102humanUncertain significance GRCh37 chr6: 145,449,900-148,319,443 , GRCh38.p12 chr6: 145,128,764-147,998,307 LOC105378039, SAMD5, 21 more genes
    nsv6136474copy number variation1nstd213human GRCh37 chr6: 146,800,000-147,020,001 , GRCh38.p12 chr6: 146,478,864-146,698,865 RAB32, ADGB, 1 more genes
    nsv4943248copy number variation1nstd200human GRCh38 chr6: 146,523,395-146,609,989 , GRCh37.p13 chr6: 146,844,531-146,931,125 RAB32, ADGB, 1 more genes
    nsv4810792copy number variation1nstd200human GRCh37 chr6: 146,812,048-146,929,037 , GRCh38.p12 chr6: 146,490,912-146,607,901 ADGB-DT, ADGB, 1 more genes
    nsv4729399copy number variation1nstd102humanUncertain significance GRCh37 chr6: 146,872,465-146,991,066 , GRCh38.p12 chr6: 146,551,329-146,669,930 ADGB, RAB32, 1 more genes
    nsv4350212copy number variation1nstd102humanPathogenic GRCh37 chr6: 135,239,633-146,997,510 , GRCh38.p12 chr6: 134,918,495-146,676,374 LOC100131041, ADGB-DT, 146 more genes
    nsv4330897inversion1nstd166human GRCh37.p13 chr6: 90,629,263-160,387,383 , GRCh38.p12 chr6: 89,919,544-159,966,351 , ACAT2, 894 more genes
    nsv4133269copy number variation1nstd166human GRCh37.p13 chr6: 146,880,988-147,017,753 , GRCh38.p12 chr6: 146,559,852-146,696,617 ADGB, ADGB-DT
    nsv3959912copy number variation1nstd168human GRCh38 chr6: 146,589,924-146,718,487 , GRCh37.p13 chr6: 146,911,060-147,039,623 ADGB, ADGB-DT
    nsv3920975copy number variation1nstd102humanPathogenic GRCh37 chr6: 141,454,127-169,739,666 , GRCh38 chr6: 141,132,990-169,339,571 , NCBI36 chr6: 141,495,820-169,481,591 UST-AS2, LOC729681, 394 more genes
    nsv3920651copy number variation1nstd102humanPathogenic GRCh38 chr6: 144,932,561-152,985,364 , NCBI36 chr6: 145,295,390-153,348,192 , GRCh37 chr6: 145,253,697-153,306,499 PPP1R14C, RAET1K, 107 more genes
    nsv3919835copy number variation1nstd102humanUncertain significance NCBI36 chr6: 146,844,177-146,975,794 , GRCh37.p13 chr6: 146,802,484-146,934,101 , GRCh38.p12 chr6: 146,481,348-146,612,965 ADGB-DT, RAB32, 1 more genes
    nsv3915150copy number variation1nstd102humanPathogenic NCBI36 chr6: 124,322,082-156,156,864 , GRCh37.p13 chr6: 124,280,383-156,115,172 , GRCh38.p12 chr6: 123,959,238-155,794,038 KATNA1, RNF217-AS1, 422 more genes
    nsv3911993copy number variation1nstd102humanPathogenic NCBI36 chr6: 133,900,102-166,209,023 , GRCh38 chr6: 133,537,271-165,875,545 , GRCh37 chr6: 133,858,409-166,289,033 LOC105369171, SHPRH, 418 more genes
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