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Items: 1 to 20 of 195

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6626758copy number variation1nstd224human GRCh37 chr20: 24,504,850-26,252,906 , GRCh38.p12 chr20: 24,524,214-26,272,270 NINL, PPIAP2, 39 more genes
    nsv6626684copy number variation1nstd224human GRCh37 chr20: 25,507,208-25,990,002 , GRCh38.p12 chr20: 25,526,572-26,009,366 MED28P7, VN1R108P, 15 more genes
    nsv6626683copy number variation1nstd224human GRCh37 chr20: 25,436,304-26,278,250 , GRCh38.p12 chr20: 25,455,668-26,297,614 NINL, FAM182A, 20 more genes
    nsv6626558copy number variation2nstd224human GRCh37 chr20: 25,829,977-25,957,014 , GRCh38.p12 chr20: 25,849,341-25,976,378 CFTRP1, LINC01733, 1 more genes
    nsv6626557copy number variation1nstd224human GRCh37 chr20: 25,650,787-25,861,259 , GRCh38.p12 chr20: 25,670,151-25,880,623 ZNF337, ZNF337-AS1, 8 more genes
    nsv6313956copy number variation1nstd102humanPathogenic GRCh37 chr20: 25,442,597-33,761,550 , GRCh38.p12 chr20: 25,461,961-35,173,747 LOC105372586, RNU6-384P, 193 more genes
    nsv6291578copy number variation1nstd102humanLikely pathogenic GRCh37 chr20: 18,665,879-33,903,216 , GRCh38.p12 chr20: 18,685,235-35,315,413 AHCY, ASIP, 330 more genes
    nsv6133911copy number variation1nstd213human GRCh37 chr20: 24,530,000-25,920,001 , GRCh38.p12 chr20: 24,549,364-25,939,365 ENTPD6, NINL, 32 more genes
    nsv6056869copy number variation1nstd212human GRCh38 chr20: 25,797,215-25,845,156 , GRCh37.p13 chr20: 25,777,851-25,825,792 FAM182B, BSNDP2, 1 more genes
    nsv5883533copy number variation2nstd209human GRCh38 chr20: 25,846,325-25,852,190 , GRCh37.p13 chr20: 25,826,961-25,832,826 LOC101926935, BSNDP2
    nsv5882777copy number variation2nstd209human GRCh38 chr20: 25,848,058-25,882,245 , GRCh37.p13 chr20: 25,828,694-25,862,881 LOC101926935
    nsv5667496inversion1nstd207human GRCh37.p13 chr20: 25,825,790-25,991,321 , GRCh38 chr20: 25,845,154-26,010,685 CFTRP1, LOC100134868, 3 more genes
    nsv5598479copy number variation1nstd207human GRCh38 chr20: 25,783,258-25,845,205 , GRCh37.p13 chr20: 25,763,894-25,825,841 FAM182B, BSNDP2, 2 more genes
    nsv5595451copy number variation1nstd207human GRCh38 chr20: 25,845,154-25,845,518 , GRCh37.p13 chr20: 25,825,790-25,826,154 BSNDP2, LOC101926935
    nsv5331834translocation1nstd200human GRCh37 chr20: 25,834,867-25,834,867 , GRCh37 chr7: 57,706,456-57,706,456 , GRCh38.p12 chr20: 25,854,231-25,854,231 , GRCh38.p12 chr7: 57,646,750-57,646,750 LOC101926935
    nsv5328014copy number variation1nstd204human GRCh38.p13 chr20: 25,516,433-25,858,450 , GRCh37.p13 chr20: 25,497,069-25,839,086 LOC107985400, LOC105372582, 12 more genes
    nsv5295140copy number variation1nstd204human GRCh38.p13 chr20: 25,847,715-25,849,468 , GRCh37.p13 chr20: 25,828,351-25,830,104 LOC101926935
    nsv5294024copy number variation1nstd204human GRCh38.p13 chr20: 25,840,301-25,847,200 , GRCh37.p13 chr20: 25,820,937-25,827,836 LOC101926935, BSNDP2
    nsv5293059copy number variation1nstd204human GRCh38.p13 chr20: 25,834,201-25,844,100 , GRCh37.p13 chr20: 25,814,837-25,824,736 BSNDP2, LOC101926935
    nsv5292935copy number variation1nstd204human GRCh38.p13 chr20: 25,802,501-25,844,100 , GRCh37.p13 chr20: 25,783,137-25,824,736 LOC101926935, BSNDP2
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