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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5493704copy number variation1nstd206human GRCh38 chr9: 65,923,095-68,291,552 , GRCh37.p13 chr9: 40,042,776-44,676,072 , CYP4F59P, 46 more genes
    nsv5482295copy number variation1nstd206human GRCh38 chr9: 66,595,387-67,865,387 , GRCh37.p13 chr9: 65,637,442-67,932,833 , FAM27B, 28 more genes
    nsv5257620copy number variation1nstd204human GRCh38.p13 chr9: 67,754,101-67,824,500 , GRCh37.p13 chr9: 67,821,547-67,891,946 , RN7SL787P
    nsv5255440copy number variation1nstd204human GRCh38.p13 chr9: 67,788,701-67,791,800 , GRCh37.p13 chr9: 67,856,147-67,859,246 RN7SL787P
    nsv5255308copy number variation1nstd204human GRCh38.p13 chr9: 67,787,001-67,791,800 , GRCh37.p13 chr9: 67,854,447-67,859,246 RN7SL787P
    nsv5252510copy number variation1nstd204human GRCh38.p13 chr9: 67,771,401-67,824,500 , GRCh37.p13 chr9: 67,838,847-67,891,946 , RN7SL787P
    nsv4766654inversion1nstd199human GRCh37 chr9: 201,453-68,434,063 , GRCh38.p12 chr9: 201,453-67,920,552 , ACO1, 876 more genes
    nsv4755256inversion1nstd199human GRCh37 chr9: 200,777-70,835,468 , GRCh38.p12 chr9: 200,777-67,920,552 , ACO1, 876 more genes
    nsv4679716copy number variation1nstd189human GRCh37.p13 chr9: 44,114,873-69,844,813 , GRCh38.p12 chr9: 40,711,180-67,920,552 , RBPJP2, 243 more genes
    nsv4675565copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-70,984,588 , GRCh38.p12 chr9: 203,861-68,369,672 LOC100132004, LOC105375993, 853 more genes
    nsv4637578copy number variation1nstd186human GRCh37 chr9: 67,854,000-67,875,000 , GRCh38.p12 chr9: 67,786,554-67,807,554 , RN7SL787P
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4457200copy number variation2nstd102humanPathogenic GRCh37 chr9: 203,861-67,986,965 , GRCh38.p12 chr9: 203,861-67,919,519 ACO1, RNU6-1073P, 846 more genes
    nsv4455152copy number variation1nstd102humanPathogenic GRCh37 chr9: 34,542,635-68,210,033 , GRCh38.p12 chr9: 34,542,637-67,920,552 FAM74A6, RGP1, 415 more genes
    nsv4436161complex substitution1nstd102humanLikely pathogenic GRCh38.p12 chr9: 23,524,428-84,744,973 , GRCh37 chr9: 23,524,426-87,359,888 ACO1, ALDH1A1, 779 more genes
    nsv4428685copy number variation1nstd174human GRCh37 chr9: 67,857,034-67,987,938 , GRCh38.p12 chr9: 67,789,588-67,920,492 , ANKRD20A1, 4 more genes
    nsv4419516copy number variation1nstd174human GRCh37 chr9: 67,809,742-67,906,255 , GRCh38.p12 chr9: 67,742,296-67,838,809 , LOC101928608, 1 more genes
    nsv4187945copy number variation1nstd166human GRCh37.p13 chr9: 67,792,000-67,963,000 , GRCh38.p12 chr9: 67,724,554-67,895,554 , ANKRD20A1, 5 more genes
    nsv4187861copy number variation1nstd166human GRCh37.p13 chr9: 67,854,000-67,875,000 , GRCh38.p12 chr9: 67,786,554-67,807,554 , RN7SL787P
    nsv4176091copy number variation1nstd166human GRCh37.p13 chr9: 67,845,400-67,987,600 , GRCh38.p12 chr9: 67,777,954-67,920,154 , ANKRD20A1, 4 more genes
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