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Items: 1 to 20 of 152

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148155copy number variation1nstd102humanPathogenic GRCh37 chr17: 72,718,277-74,142,256 , GRCh38.p12 chr17: 74,722,138-76,146,175 TRIM65, TEN1, 74 more genes
    nsv7098900copy number variation1nstd102humanUncertain significance GRCh37 chr17: 72,864,876-73,328,878 , GRCh38.p12 chr17: 74,868,753-75,332,797 CDR2L, OTOP2, 28 more genes
    nsv6990700copy number variation1nstd229human GRCh38 chr17: 75,270,468-75,275,629 , GRCh37.p13 chr17: 73,266,549-73,271,710 MIF4GD-DT, SLC25A19, 1 more genes
    nsv6984264copy number variation1nstd229human GRCh38 chr17: 74,239,313-78,611,254 , GRCh37.p13 chr17: 72,235,452-76,607,336 SNORD1C, PRCD, 178 more genes
    nsv6580372inversion1nstd223human GRCh38 chr17: 72,236,607-79,483,477 , GRCh37.p13 chr17: 70,232,748-77,412,076 TNRC6C, PTMAP13, 217 more genes
    nsv6530329copy number variation1nstd223human GRCh38 chr17: 75,256,379-75,325,276 , GRCh37.p13 chr17: 73,252,460-73,321,357 GRB2, MRPS7, 4 more genes
    nsv6526494copy number variation1nstd223human GRCh38 chr17: 75,270,468-75,275,626 , GRCh37.p13 chr17: 73,266,549-73,271,707 MIF4GD, SLC25A19, 1 more genes
    nsv6314018copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,049,227-73,533,226 , GRCh38.p12 chr17: 75,053,132-75,537,145 MIF4GD-DT, TSEN54, 21 more genes
    nsv6310407copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,204,602-73,515,148 , GRCh38.p12 chr17: 75,208,507-75,519,067 CASKIN2, MRPS7, 12 more genes
    nsv6291659copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,045,938-73,310,951 , GRCh38.p12 chr17: 75,049,843-75,314,870 SLC25A19, NUP85, 12 more genes
    nsv6133070copy number variation1nstd213human GRCh37 chr17: 62,460,000-73,800,001 , GRCh38.p12 chr17: 64,464,645-75,803,920 APOH, CACNG1, 225 more genes
    nsv5293343copy number variation1nstd204human GRCh38.p13 chr17: 74,899,101-76,684,700 , GRCh37.p13 chr17: 72,895,199-74,680,782 , RNU6-24P, 92 more genes
    nsv5285175copy number variation1nstd204human GRCh38.p13 chr17: 75,213,501-75,463,000 , GRCh37.p13 chr17: 73,209,596-73,459,081 MIR3678, MIF4GD-DT, 9 more genes
    nsv5016676copy number variation1nstd200human GRCh38 chr17: 75,270,468-75,275,626 , GRCh37.p13 chr17: 73,266,549-73,271,707 MIF4GD-DT, SLC25A19, 1 more genes
    nsv5014010copy number variation1nstd200human GRCh38 chr17: 75,062,121-75,491,883 , GRCh37.p13 chr17: 73,058,216-73,487,964 NUP85, RNU6-938P, 17 more genes
    nsv4854385copy number variation1nstd200human GRCh37 chr17: 73,058,216-73,487,964 , GRCh38.p12 chr17: 75,062,121-75,491,883 LOC107985034, SUMO2, 17 more genes
    nsv4676207copy number variation1nstd102humanUncertain significance GRCh37 chr17: 73,218,219-73,443,987 , GRCh38.p12 chr17: 75,222,124-75,447,906 GGA3, TMEM94, 9 more genes
    nsv4676145copy number variation1nstd102humanUncertain significance GRCh37 chr17: 72,945,415-73,414,786 , GRCh38.p12 chr17: 74,949,320-75,418,705 MIF4GD-DT, NT5C, 27 more genes
    nsv4676104copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,261,871-78,608,763 , GRCh38.p12 chr17: 75,265,790-80,634,963 LLGL2, TSEN54, 165 more genes
    nsv4628995copy number variation1nstd183human GRCh37 chr17: 73,217,773-73,774,243 , GRCh38.p12 chr17: 75,221,678-75,778,162 , LOC107985013, 23 more genes
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