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Items: 1 to 20 of 26

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3923205copy number variation1nstd102humanPathogenic NCBI36 chr22: 25,177,008-30,177,912 , GRCh37 chr22: 26,847,008-31,847,912 , GRCh38 chr22: 26,451,042-31,451,926 TFIP11, DRG1, 138 more genes
    nsv3924941copy number variation1nstd102humanPathogenic GRCh38 chr22: 26,221,273-29,477,543 , GRCh37 chr22: 26,617,239-29,873,532 , NCBI36 chr22: 24,947,239-28,203,532 TFIP11, RASL10A, 66 more genes
    nsv6637977copy number variation1nstd102humanPathogenic GRCh37 chr22: 26,614,429-29,847,680 , GRCh38.p12 chr22: 26,218,463-29,451,691 TFIP11, MIAT, 65 more genes
    nsv4676280copy number variation1nstd102humanPathogenic GRCh37 chr22: 26,337,910-28,489,947 , GRCh38.p12 chr22: 25,941,943-28,093,959 TFIP11, LOC646216, 42 more genes
    nsv3902776copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,054,667-51,243,435 , GRCh38.p12 chr22: 16,367,190-50,805,007 TFIP11, LOC100419811, 1084 more genes
    nsv3894026copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,054,691-51,237,518 , GRCh38.p12 chr22: 16,367,190-50,799,090 TFIP11, IGKV3OR22-2, 1084 more genes
    nsv3890411copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,054,691-51,237,463 , GRCh38.p12 chr22: 16,367,190-50,799,035 TFIP11, RNU6-495P, 1084 more genes
    nsv4729926copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,197,005-51,224,252 , GRCh38.p12 chr22: 16,367,190-50,785,824 TFIP11, FBXO7, 1084 more genes
    nsv3902598copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,054,691-51,220,902 , GRCh38.p12 chr22: 16,367,190-50,782,474 TFIP11, FABP5P11, 1084 more genes
    nsv3907231copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,114,244-51,211,392 , GRCh38.p12 chr22: 16,367,190-50,772,964 TFIP11, DDTL, 1084 more genes
    nsv3890401copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,114,244-51,195,728 , GRCh38.p12 chr22: 16,367,190-50,757,300 TFIP11, YPEL1, 1083 more genes
    nsv4457771copy number variation1nstd102humanPathogenic GRCh37 chr22: 16,888,899-51,197,838 , GRCh38.p12 chr22: 16,408,173-50,759,410 TFIP11, IGLV3-27, 1082 more genes
    nsv3891895copy number variation2nstd102humanPathogenic GRCh37 chr22: 16,888,900-51,197,838 , GRCh38.p12 chr22: 16,408,174-50,759,410 TFIP11, POM121L7P, 1082 more genes
    nsv3913775copy number variation1nstd102humanPathogenic NCBI36 chr22: 15,777,498-49,525,130 , GRCh38 chr22: 16,916,608-50,739,836 , GRCh37 chr22: 17,397,498-51,178,264 TFIP11, ZNF280A, 1059 more genes
    nsv3919881copy number variation1nstd102humanPathogenic GRCh37 chr22: 17,397,633-51,178,213 , GRCh38 chr22: 16,916,743-50,739,785 , NCBI36 chr22: 15,777,633-49,525,079 TFIP11, MIR12114, 1059 more genes
    nsv3919085copy number variation1nstd102humanPathogenic NCBI36 chr22: 17,008,132-49,591,432 , GRCh37.p13 chr22: 18,628,132-51,244,566 , GRCh38.p12 chr22: 18,145,365-50,806,138 TFIP11, IGLV2-28, 1023 more genes
    nsv3914617copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,261,514-37,583,387 , GRCh38 chr22: 20,907,226-37,187,347 , NCBI36 chr22: 19,591,514-35,913,333 TFIP11, RASL10A, 525 more genes
    nsv3919429copy number variation1nstd102humanPathogenic GRCh37 chr22: 18,661,724-32,217,179 , GRCh38 chr22: 18,178,957-31,821,193 , NCBI36 chr22: 17,041,724-30,547,179 TFIP11, PCAT14, 533 more genes
    nsv3922708copy number variation1nstd102humanPathogenic GRCh38 chr22: 23,279,231-36,247,369 , GRCh37 chr22: 23,621,418-36,643,415 , NCBI36 chr22: 21,951,418-34,973,361 TFIP11, DRICH1, 316 more genes
    nsv3901960copy number variation1nstd102humanPathogenic GRCh37 chr22: 23,637,907-36,614,412 , GRCh38.p12 chr22: 23,295,720-36,218,366 TFIP11, GRK3, 314 more genes
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