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Items: 1 to 20 of 74

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6291579copy number variation1nstd102humanLikely benign GRCh37 chr16: 4,180,337-4,246,982 , GRCh38.p12 chr16: 4,130,336-4,196,981 SRL, DBIP3, 1 more genes
    nsv3894483copy number variation1nstd102humanBenign GRCh37 chr14: 24,426,950-24,484,346 , GRCh38.p12 chr14: 23,957,741-24,015,137 , GRCh38.p12 chr14|NW_018654722.1: 258,720-316,310 DHRS4, DHRS4L2, 1 more genes
    nsv3890915copy number variation1nstd102humanBenign GRCh37 chr14: 24,435,564-24,480,555 , GRCh38.p12 chr14: 23,966,355-24,011,346 , GRCh38.p12 chr14|NW_018654722.1: 267,333-316,310 DHRS4L1, DHRS4, 1 more genes
    nsv3895315copy number variation1nstd102humanUncertain significance GRCh37 chr16: 4,010,729-4,300,636 , GRCh38.p12 chr16: 3,960,728-4,250,635 SRL, LOC105371062, 3 more genes
    nsv3874585copy number variation1nstd102humanUncertain significance GRCh37 chr16: 4,264,335-4,387,622 , GRCh38 chr16: 4,214,334-4,337,621 SRL, LINC01569, 3 more genes
    nsv4674832copy number variation1nstd102humanUncertain significance GRCh37 chr16: 4,202,558-4,299,830 , GRCh38.p12 chr16: 4,152,557-4,249,829 SRL, LOC105371062, 1 more genes
    nsv6314715copy number variation1nstd102humanPathogenic GRCh37 chr14: 21,162,263-50,713,602 , GRCh38.p12 chr14: 20,694,104-50,246,884 HNRNPC, FOXG1, 616 more genes
    nsv3916277copy number variation1nstd102humanPathogenic NCBI36 chr14: 19,734,944-44,823,755 , GRCh38 chr14: 20,196,945-45,284,802 , GRCh37 chr14: 20,665,104-45,754,005 MIR208B, MRPL52, 600 more genes
    nsv3917157copy number variation1nstd102humanPathogenic GRCh37 chr14: 24,018,169-42,452,605 , GRCh38 chr14: 23,548,960-41,983,402 , NCBI36 chr14: 23,088,009-41,522,355 LINC02300, COCH, 274 more genes
    nsv3896078copy number variation1nstd102humanPathogenic GRCh37 chr14: 24,233,721-31,377,083 , GRCh38.p12 chr14: 23,864,182-30,907,877 PSME1, EIF4A1P12, 107 more genes
    nsv3912877copy number variation1nstd102humanPathogenic GRCh37 chr16: 2,900,735-7,160,698 , NCBI36 chr16: 2,840,736-7,100,699 , GRCh38 chr16: 2,850,734-7,110,697 SRL, TRP-CGG1-2, 129 more genes
    nsv3909798copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,146,027-6,362,229 , GRCh38.p12 chr16: 3,096,026-6,312,228 SRL, LINC01569, 102 more genes
    nsv4453988copy number variation1nstd102humanPathogenic GRCh38 chr16: 3,727,698-4,802,591 , GRCh37 chr16: 3,777,699-4,852,592 SRL, RN7SL850P, 30 more genes
    nsv3923111copy number variation1nstd102humanPathogenic NCBI36 chr16: 3,810,524-4,658,349 , GRCh37 chr16: 3,870,523-4,718,348 , GRCh38 chr16: 3,820,522-4,668,347 SRL, UBALD1, 21 more genes
    nsv6314863copy number variation1nstd102humanPathogenic GRCh38 chr16: 3,619,617-4,448,281 , GRCh37.p13 chr16: 3,669,618-4,498,282 SRL, TRAP1, 15 more genes
    nsv3917367copy number variation1nstd102humanPathogenic GRCh38 chr16: 3,560,564-4,266,796 , GRCh37 chr16: 3,610,565-4,316,797 , NCBI36 chr16: 3,550,566-4,256,798 SRL, TRAP1, 11 more genes
    nsv4683275copy number variation1nstd102humanPathogenic GRCh37 chr16: 3,794,875-4,387,545 , GRCh38.p12 chr16: 3,744,874-4,337,544 SRL, GLIS2-AS1, 8 more genes
    nsv3906108copy number variation1nstd102humanPathogenic GRCh37 chr16: 61,451-90,294,632 , GRCh38.p12 chr16: 11,451-90,228,224 SRL, CKLF, 1882 more genes
    nsv3904593copy number variation1nstd102humanPathogenic GRCh37 chr16: 69,193-90,274,381 , GRCh38.p12 chr16: 19,193-90,207,973 SRL, LOC100128079, 1879 more genes
    nsv3901410copy number variation1nstd102humanPathogenic GRCh37 chr16: 88,165-90,274,695 , GRCh38.p12 chr16: 38,165-90,208,287 SRL, LINC02175, 1877 more genes
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