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Items: 1 to 20 of 35

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3897748copy number variation1nstd102humanBenign GRCh37 chr17: 78,157,811-78,169,375 , GRCh38.p12 chr17: 80,184,012-80,195,576 CARD14
    nsv7093272copy number variation1nstd102humanUncertain significance GRCh38 chr17: 80,198,528-80,198,619 , GRCh37 chr17: 78,172,327-78,172,418 CARD14
    nsv7095421copy number variation1nstd102humanUncertain significance GRCh37 chr17: 78,155,238-78,166,438 , GRCh38.p12 chr17: 80,181,439-80,192,639 CARD14
    nsv7095367copy number variation1nstd102humanUncertain significance GRCh37 chr17: 78,177,655-78,183,100 , GRCh38.p12 chr17: 80,203,856-80,209,301 CARD14, SGSH
    nsv5381257copy number variation1nstd102humanUncertain significance GRCh37 chr17: 78,155,218-78,172,575 , GRCh38.p12 chr17: 80,181,419-80,198,776 CARD14, SGSH
    nsv6310341copy number variation1nstd102humanUncertain significance GRCh37 chr17: 78,168,970-78,182,144 , GRCh38.p12 chr17: 80,195,171-80,208,345 CARD14, SGSH
    nsv7094991copy number variation1nstd102humanUncertain significance GRCh37 chr17: 78,177,601-78,179,471 , GRCh38.p12 chr17: 80,203,802-80,205,672 CARD14, SGSH
    nsv7094925copy number variation1nstd102humanUncertain significance GRCh37 chr17: 78,109,289-78,272,338 , GRCh38.p12 chr17: 80,135,490-80,298,538 CARD14, RNF213, 3 more genes
    nsv6310240copy number variation1nstd102humanUncertain significance GRCh37 chr17: 78,010,462-78,158,057 , GRCh38.p12 chr17: 80,036,663-80,184,258 CARD14, GAA, 3 more genes
    nsv6310339copy number variation1nstd102humanUncertain significance GRCh37 chr17: 78,032,273-78,163,691 , GRCh38.p12 chr17: 80,058,474-80,189,892 CARD14, EIF4A3, 3 more genes
    nsv3911811copy number variation1nstd102humanPathogenic NCBI36 chr17: 31,824,931-78,654,742 , GRCh37.p13 chr17: 34,750,818-81,048,189 , GRCh38.p12 chr17: 36,382,248-83,103,577 CARD14, PRPSAP1, 1350 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 CARD14, MIR3185, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 CARD14, P4HB, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 CARD14, MIR21, 2366 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 CARD14, SMURF2, 2366 more genes
    nsv3914783copy number variation1nstd102humanPathogenic NCBI36 chr17: 16,698,288-78,654,742 , GRCh37.p13 chr17: 16,757,563-81,048,189 , GRCh38.p12 chr17: 16,854,249-83,103,577 CARD14, LOC105371922, 1855 more genes
    nsv3909511copy number variation1nstd102humanPathogenic GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846 CARD14, FOXK2, 958 more genes
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 CARD14, LOC107985089, 448 more genes
    nsv3909523copy number variation1nstd102humanPathogenic GRCh37 chr17: 63,689,671-81,041,938 , GRCh38.p12 chr17: 65,693,553-83,084,062 CARD14, RPL38, 428 more genes
    nsv3906075copy number variation1nstd102humanPathogenic GRCh37 chr17: 67,002,415-81,041,938 , GRCh38.p12 chr17: 69,006,274-83,084,062 CARD14, CEP131, 374 more genes
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