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Items: 1 to 20 of 311

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096339copy number variation1nstd102humanUncertain significance GRCh37 chr22: 22,277,465-22,300,420 , GRCh38.p12 chr22: 21,923,092-21,946,048 PPM1F-AS1, PPM1F
    nsv7024377copy number variation1nstd229human GRCh38 chr22: 21,933,270-21,937,387 , GRCh37.p13 chr22: 22,287,642-22,291,759 PPM1F, PPM1F-AS1
    nsv7023906copy number variation1nstd229human GRCh38 chr22: 21,897,748-21,990,276 , GRCh37.p13 chr22: 22,252,086-22,344,673 PPM1F-AS1, TOP3B, 2 more genes
    nsv7023486copy number variation1nstd229human GRCh38 chr22: 21,868,886-21,944,065 , GRCh37.p13 chr22: 22,223,176-22,298,437 PPM1F-AS1, PPM1F
    nsv6637518copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,029,656-22,485,776 , GRCh38.p12 chr22: 20,675,368-22,131,383 ABHD17AP5, MIR301B, 70 more genes
    nsv6637335copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,465,662-22,962,962 , GRCh38.p12 chr22: 21,111,373-22,620,492 ABHD17AP5, UBE2L3, 97 more genes
    nsv6635892copy number variation1nstd227human GRCh38.p12 chr22: 21,941,747-22,219,245 , GRCh37 chr22: 22,296,119-22,573,637 IGL, TOP3B, 28 more genes
    nsv6635183copy number variation1nstd227human GRCh38.p12 chr22: 21,936,031-22,230,413 , GRCh37 chr22: 22,290,403-22,584,809 IGL, TOP3B, 30 more genes
    nsv6635080copy number variation1nstd227human GRCh38.p12 chr22: 21,682,223-22,230,413 , GRCh37 chr22: 22,036,512-22,584,809 IGL, MAPK1, 35 more genes
    nsv6634914copy number variation1nstd227human GRCh38.p12 chr22: 21,700,991-22,230,413 , GRCh37 chr22: 22,055,280-22,584,809 IGL, MAPK1, 34 more genes
    nsv6627184copy number variation1nstd224human GRCh37 chr22: 21,799,719-23,803,722 , GRCh38.p12 chr22: 21,445,430-23,461,535 BCRP4, GNAZ, 158 more genes
    nsv6627051copy number variation1nstd224human GRCh37 chr22: 22,260,441-22,292,217 , GRCh38.p12 chr22: 21,906,101-21,937,845 PPM1F, PPM1F-AS1
    nsv6540095copy number variation1nstd223human GRCh38 chr22: 20,268,331-23,402,807 , GRCh37.p13 chr22: 20,255,854-23,744,994 IGLC2, IGLVIV-53, 214 more genes
    nsv6315562copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,798,906-25,039,018 , GRCh38.p12 chr22: 21,444,617-24,643,051 IGLVI-42, ADORA2A-AS1, 205 more genes
    nsv6315480copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,462,566-22,962,196 , GRCh38.p12 chr22: 21,108,277-22,619,726 IGLV8-61, SDF2L1, 97 more genes
    nsv6314782copy number variation1nstd220human GRCh38.p12 chr22: 21,351,861-24,248,764 , GRCh37 chr22: 21,706,150-24,644,732 ASLP1, BCR, 195 more genes
    nsv6291785copy number variation1nstd102humanUncertain significance GRCh37 chr22: 21,974,641-22,401,879 , GRCh38.p12 chr22: 21,620,352-22,047,481 IGL, CCDC116, 19 more genes
    nsv6291464copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,465,661-24,631,791 , GRCh38.p12 chr22: 21,111,372-24,235,823 IGLVIV-64, FAM230B, 205 more genes
    nsv6290344copy number variation1nstd102humanUncertain significance GRCh37 chr22: 21,905,051-22,989,041 , GRCh38.p12 chr22: 21,550,762-22,646,571 IGLV1-47, LOC100736408, 81 more genes
    nsv6289929copy number variation1nstd102humanPathogenic GRCh37 chr22: 21,514,655-22,986,816 , GRCh38.p12 chr22: 21,160,366-22,644,345 IGLV9-49, BCRP6, 97 more genes
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