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Items: 1 to 20 of 371

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7077086inversion1nstd229human GRCh38 chr14: 30,623,924-30,623,938 , GRCh37.p13 chr14: 31,093,130-31,093,144 SCFD1
    nsv6957819copy number variation1nstd229human GRCh38 chr14: 29,967,815-31,229,292 , GRCh37.p13 chr14: 30,437,021-31,698,498 LOC100913082, RPS6P24, 19 more genes
    nsv6955310copy number variation1nstd229human GRCh38 chr14: 30,646,320-30,646,402 , GRCh37.p13 chr14: 31,115,526-31,115,608 SCFD1
    nsv6949960copy number variation1nstd229human GRCh38 chr14: 30,663,649-30,666,920 , GRCh37.p13 chr14: 31,132,855-31,136,126 SCFD1
    nsv6941159copy number variation1nstd229human GRCh38 chr14: 30,664,701-30,668,000 , GRCh37.p13 chr14: 31,133,907-31,137,206 SCFD1
    nsv6938586copy number variation1nstd229human GRCh38 chr14: 30,735,849-30,738,422 , GRCh37.p13 chr14: 31,205,055-31,207,628 SCFD1
    nsv6637416copy number variation1nstd102humanPathogenic GRCh37 chr14: 24,959,823-33,415,359 , GRCh38.p12 chr14: 24,490,617-32,946,153 SCFD1, RPL12P5, 94 more genes
    nsv6591606inversion1nstd223human GRCh38 chr14: 30,656,873-33,818,146 , GRCh37.p13 chr14: 31,126,079-34,287,352 ARHGAP5-AS1, RN7SL660P, 37 more genes
    nsv6491050copy number variation1nstd223human GRCh38 chr14: 30,712,501-30,716,100 , GRCh37.p13 chr14: 31,181,707-31,185,306 SCFD1
    nsv6489885copy number variation1nstd223human GRCh38 chr14: 30,640,501-30,641,000 , GRCh37.p13 chr14: 31,109,707-31,110,206 SCFD1
    nsv6489004copy number variation1nstd223human GRCh38 chr14: 30,719,993-30,721,131 , GRCh37.p13 chr14: 31,189,199-31,190,337 SCFD1
    nsv6479969copy number variation1nstd223human GRCh38 chr14: 30,721,801-30,723,000 , GRCh37.p13 chr14: 31,191,007-31,192,206 SCFD1
    nsv6479768copy number variation1nstd223human GRCh38 chr14: 30,735,724-30,736,411 , GRCh37.p13 chr14: 31,204,930-31,205,617 SCFD1
    nsv6476617copy number variation1nstd223human GRCh38 chr14: 30,672,582-30,672,965 , GRCh37.p13 chr14: 31,141,788-31,142,171 SCFD1
    nsv6315513copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,672-47,481,203 , GRCh38.p12 chr14: 20,043,513-47,012,000 CDH24, KLHL33, 623 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
    nsv6258659mobile element insertion1nstd215human GRCh38 chr14: 30,712,073-30,712,073 , GRCh37.p13 chr14: 31,181,279-31,181,279 SCFD1
    nsv6258658mobile element insertion1nstd215human GRCh38 chr14: 30,679,111-30,679,111 , GRCh37.p13 chr14: 31,148,317-31,148,317 SCFD1
    nsv6204753copy number variation1nstd214human GRCh38 chr14: 30,625,599-30,625,654 , GRCh37.p13 chr14: 31,094,805-31,094,860 SCFD1
    nsv6195567copy number variation1nstd214human GRCh38 chr14: 30,677,783-30,677,844 , GRCh37.p13 chr14: 31,146,989-31,147,050 SCFD1
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