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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5372546translocation1nstd200human GRCh38 chr9: 69,016,712-69,016,712 , GRCh38 chr9: 69,014,257-69,014,257 , GRCh37.p13 chr9: 71,631,628-71,631,628 , GRCh37.p13 chr9: 71,629,173-71,629,173 PRKACG
    nsv5372545translocation1nstd200human GRCh38 chr9: 69,018,747-69,018,747 , GRCh38 chr9: 69,014,159-69,014,159 , GRCh37.p13 chr9: 71,629,075-71,629,075 , GRCh37.p13 chr9: 71,633,663-71,633,663 PRKACG
    nsv5336520translocation1nstd200human GRCh37 chr9: 71,633,663-71,633,663 , GRCh37 chr9: 71,629,075-71,629,075 , GRCh38.p12 chr9: 69,014,159-69,014,159 , GRCh38.p12 chr9: 69,018,747-69,018,747 PRKACG
    nsv5331466translocation1nstd200human GRCh37 chr9: 71,629,173-71,629,173 , GRCh37 chr9: 71,631,628-71,631,628 , GRCh38.p12 chr9: 69,014,257-69,014,257 , GRCh38.p12 chr9: 69,016,712-69,016,712 PRKACG
    nsv4954796copy number variation1nstd200human GRCh38 chr9: 68,989,021-69,011,864 , GRCh37.p13 chr9: 71,603,937-71,626,780 PRKACG, PIP5K1B
    nsv4954795copy number variation1nstd200human GRCh38 chr9: 68,982,687-69,234,462 , GRCh37.p13 chr9: 71,597,603-71,849,378 FXN, PIP5K1B, 2 more genes
    nsv4954793copy number variation1nstd200human GRCh38 chr9: 68,885,222-69,216,235 , GRCh37.p13 chr9: 71,500,138-71,831,151 LOC101927069, PRKACG, 4 more genes
    nsv4954792copy number variation1nstd200human GRCh38 chr9: 68,780,692-69,356,269 , GRCh37.p13 chr9: 71,395,608-71,971,185 BANCR, LOC101927069, 8 more genes
    nsv4814768copy number variation1nstd200human GRCh37 chr9: 71,597,603-71,849,378 , GRCh38.p12 chr9: 68,982,687-69,234,462 PRKACG, TJP2, 2 more genes
    nsv4679593copy number variation1nstd189human GRCh37.p13 chr9: 71,542,353-71,805,433 , GRCh38.p12 chr9: 68,927,437-69,190,517 FXN, PRKACG, 4 more genes
    nsv4604106copy number variation1nstd183human GRCh37 chr9: 71,433,392-71,901,672 , GRCh38.p12 chr9: 68,818,476-69,286,756 FXN, PRKACG, 4 more genes
    nsv4457273copy number variation1nstd102humanPathogenic GRCh37 chr9: 203,861-141,020,388 , GRCh38.p12 chr9: 203,861-138,125,936 CDRT15P14, MIR548AW, 2167 more genes
    nsv4456755copy number variation1nstd102humanUncertain significance GRCh37 chr9: 71,458,419-71,776,105 , GRCh38.p12 chr9: 68,843,503-69,161,189 PRKACG, LOC101927069, 4 more genes
    nsv4456741copy number variation1nstd102humanUncertain significance GRCh37 chr9: 71,415,902-71,996,013 , GRCh38.p12 chr9: 68,800,986-69,381,097 LOC101927069, BANCR, 6 more genes
    nsv4456270copy number variation1nstd102humanUncertain significance GRCh37 chr9: 71,415,902-71,971,195 , GRCh38.p12 chr9: 68,800,986-69,356,279 LOC101927069, PRKACG, 6 more genes
    nsv4456047copy number variation1nstd102humanUncertain significance GRCh37 chr9: 71,221,738-71,660,766 , GRCh38.p12 chr9: 68,606,822-69,045,850 LOC105376071, PABIR1, 8 more genes
    nsv4455928copy number variation1nstd102humanPathogenic GRCh37 chr9: 70,974,661-81,829,792 , GRCh38.p12 chr9: 68,359,745-79,214,877 RPL35AP21, LOC105376097, 134 more genes
    nsv4455804copy number variation1nstd102humanUncertain significance GRCh37 chr9: 71,533,382-71,987,060 , GRCh38.p12 chr9: 68,918,466-69,372,144 RNU6-820P, PIP5K1B, 6 more genes
    nsv4455186copy number variation1nstd102humanPathogenic GRCh37 chr9: 71,416,475-141,020,389 , GRCh38.p12 chr9: 68,801,559-138,125,937 LOC105376327, ENG, 1304 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
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