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Items: 1 to 20 of 571

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5381674copy number variation1nstd102humanPathogenic GRCh37 chrX: 7,137,497-7,272,667 , GRCh38.p12 chrX: 7,219,456-7,354,626 STS
    nsv6313234copy number variation2nstd102humanUncertain significance, Pathogenic GRCh37 chrX: 7,137,717-7,268,302 , GRCh38.p12 chrX: 7,219,676-7,350,261 STS
    nsv5381753copy number variation1nstd102humanPathogenic GRCh37 chrX: 7,137,717-7,268,302 , GRCh38.p12 chrX: 7,219,676-7,350,261 STS
    nsv3885671copy number variation1nstd102humanPathogenic GRCh37 chrX: 7,143,912-7,185,127 , GRCh38.p12 chrX: 7,225,871-7,267,086 STS
    nsv3891337copy number variation1nstd102humanPathogenic GRCh37 chrX: 7,145,359-7,177,501 , GRCh38 chrX: 7,227,318-7,259,460 , NCBI36 chrX: 7,155,359-7,187,501 STS
    nsv7098545copy number variation1nstd102humanLikely pathogenic GRCh37 chrX: 7,171,217-7,177,833 , GRCh38.p12 chrX: 7,253,176-7,259,792 STS
    nsv3885862copy number variation1nstd102humanBenign GRCh37 chrX: 7,269,569-7,706,446 , GRCh38.p12 chrX: 7,351,528-7,738,405 STS
    nsv3870534copy number variation1nstd102humanBenign GRCh37 chrX: 7,218,800-7,391,581 , GRCh38.p12 chrX: 7,300,759-7,473,540 STS
    nsv3880064copy number variation1nstd102humanBenign GRCh37 chrX: 7,113,308-7,255,259 , GRCh38.p12 chrX: 7,195,267-7,337,218 STS
    nsv4728673copy number variation1nstd102humanUncertain significance GRCh37 chrX: 7,168,745-7,754,214 , GRCh38.p12 chrX: 7,250,704-7,786,173 STS
    nsv3872687copy number variation1nstd102humanUncertain significance GRCh37 chrX: 7,153,846-7,469,635 , GRCh38.p12 chrX: 7,235,805-7,551,594 STS
    nsv3900409copy number variation1nstd102humanUncertain significance NCBI36 chrX: 7,225,335-7,409,734 , GRCh37 chrX: 7,215,335-7,399,734 , GRCh38 chrX: 7,297,294-7,481,693 STS
    nsv3897999copy number variation1nstd102humanUncertain significance NCBI36 chrX: 7,078,722-7,253,344 , GRCh38 chrX: 7,150,681-7,325,303 , GRCh37 chrX: 7,068,722-7,243,344 STS
    nsv3873073copy number variation1nstd102humanUncertain significance GRCh37 chrX: 7,252,959-7,394,015 , GRCh38.p12 chrX: 7,334,918-7,475,974 STS
    nsv4674520copy number variation1nstd102humanUncertain significance GRCh37 chrX: 7,252,959-7,391,892 , GRCh38.p12 chrX: 7,334,918-7,473,851 STS
    nsv4728389copy number variation1nstd102humanUncertain significance GRCh37 chrX: 7,266,135-7,391,892 , GRCh38.p12 chrX: 7,348,094-7,473,851 STS
    nsv4728185copy number variation1nstd102humanUncertain significance GRCh37 chrX: 7,266,135-7,366,211 , GRCh38.p12 chrX: 7,348,094-7,448,170 STS
    nsv7098328copy number variation1nstd102humanUncertain significance GRCh37 chrX: 7,223,067-7,268,302 , GRCh38.p12 chrX: 7,305,026-7,350,261 STS
    nsv3879598copy number variation1nstd102humanLikely benign GRCh37 chrX: 7,236,970-7,828,792 , GRCh38.p12 chrX: 7,318,929-7,860,751 STS, VCX
    nsv4457617copy number variation1nstd102humanUncertain significance GRCh37 chr21: 43,852,444-43,913,048 , GRCh38.p12 chr21: 42,432,335-42,492,938 RSPH1, UBASH3A
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