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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6289812copy number variation1nstd102humanPathogenic GRCh37 chr8: 11,667,760-11,787,743 , GRCh38.p12 chr8: 11,810,251-11,930,234 , GRCh38.p12 chr8|NW_018654717.1: 1,417,798-1,537,843 FDFT1, OR7E161P, 2 more genes
    nsv3877451copy number variation1nstd102humanLikely pathogenic GRCh37 chr8: 11,667,760-11,787,743 , GRCh38 chr8: 11,810,251-11,930,234 FDFT1, CTSB, 2 more genes
    nsv3910338copy number variation1nstd102humanLikely benign NCBI36 chr8: 11,668,689-11,716,112 , GRCh37 chr8: 11,631,280-11,678,703 , GRCh38 chr8: 11,773,771-11,821,194 FDFT1, NEIL2, 2 more genes
    nsv3895792copy number variation1nstd102humanLikely benign GRCh37 chr8: 11,640,871-11,651,233 , GRCh38.p12 chr8: 11,783,362-11,793,724 , GRCh38.p12 chr8|NW_018654717.1: 1,554,375-1,564,736 FDFT1, LOC105379243, 2 more genes
    nsv3915141copy number variation1nstd102humanUncertain significance NCBI36 chr8: 11,676,388-11,762,347 , GRCh37.p13 chr8: 11,638,979-11,724,938 , GRCh38.p12 chr8: 11,781,470-11,867,429 , GRCh38.p12 chr8|NW_018654717.1: 1,480,630-1,566,628 FDFT1, SUB1P1, 3 more genes
    nsv4457113copy number variation1nstd102humanUncertain significance GRCh37 chr8: 11,632,835-11,682,672 , GRCh38.p12 chr8: 11,775,326-11,825,163 , GRCh38.p12 chr8|NW_018654717.1: 1,522,930-1,572,774 FDFT1, SUB1P1, 2 more genes
    nsv3894801copy number variation1nstd102humanPathogenic GRCh37 chr8: 11,608,214-11,683,083 , GRCh38.p12 chr8: 11,750,705-11,825,574 , GRCh38.p12 chr8|NW_018654717.1: 1,522,520-1,597,379 FDFT1, GATA4, 4 more genes
    nsv3910925copy number variation1nstd102humanPathogenic NCBI36 chr8: 11,634,153-11,698,352 , GRCh37 chr8: 11,596,744-11,660,943 , GRCh38 chr8: 11,739,235-11,803,434 FDFT1, GATA4, 4 more genes
    nsv6315449copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-30,187,456 , GRCh38.p12 chr8: 208,048-30,329,940 FDFT1, LOC101928016, 568 more genes
    nsv3917350copy number variation2nstd102humanPathogenic GRCh37 chr8: 2,292,235-27,361,796 , GRCh38 chr8: 2,475,295-27,504,279 , NCBI36 chr8: 2,121,457-27,417,713 FDFT1, LINC03022, 472 more genes
    nsv7148253copy number variation1nstd102humanPathogenic GRCh38 chr8: 449,893-23,854,904 , GRCh37.p13 chr8: 399,893-23,712,417 FDFT1, ENTPD4, 447 more genes
    nsv6636968copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,049-18,936,715 , GRCh38.p12 chr8: 208,049-19,079,205 FDFT1, ZNF705B, 357 more genes
    nsv4455719copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-14,214,722 , GRCh38.p12 chr8: 208,048-14,357,213 FDFT1, MIR598, 312 more genes
    nsv6636940copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,049-10,965,627 , GRCh38.p12 chr8|NW_018654717.1: 1-5,513,617 , GRCh38.p12 chr8: 208,049-11,108,117 FDFT1, HSPD1P3, 270 more genes
    nsv3902717copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-10,939,681 , GRCh38.p12 chr8: 208,048-11,082,171 , GRCh38.p12 chr8|NW_018654717.1: 1-5,513,617 FDFT1, LOC101929128, 270 more genes
    nsv3900231copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,213-10,197,718 , GRCh38.p12 chr8|NW_018654717.1: 1-5,513,617 , GRCh38.p12 chr8: 60,213-10,340,208 FDFT1, LOC105377793, 273 more genes
    nsv3914458copy number variation1nstd102humanPathogenic NCBI36 chr8: 7,079,769-12,416,695 , GRCh38 chr8: 7,234,837-12,514,815 , GRCh37 chr8: 7,092,359-12,372,324 FDFT1, DEFB103B, 191 more genes
    nsv3917857copy number variation1nstd102humanPathogenic NCBI36 chr8: 7,040,596-12,285,523 , GRCh38 chr8: 7,195,664-12,383,643 , GRCh37 chr8: 7,053,186-12,241,152 FDFT1, MIR124-1, 185 more genes
    nsv3916612copy number variation1nstd102humanPathogenic NCBI36 chr8: 7,256,229-11,843,369 , GRCh37.p13 chr8: 7,268,819-11,805,960 , GRCh38.p12 chr8: 7,411,297-11,948,451 , GRCh38.p12 chr8|NW_018654717.1: 655,251-5,419,355 FDFT1, DEFB107A, 167 more genes
    nsv3912043copy number variation1nstd102humanPathogenic GRCh38 chr8: 7,411,297-11,961,807 , NCBI36 chr8: 7,256,229-11,856,725 , GRCh37 chr8: 7,268,819-11,819,316 FDFT1, LOC105379241, 138 more genes
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