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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6992139copy number variation1nstd229human GRCh38 chr17: 58,169,406-58,175,516 , GRCh37.p13 chr17: 56,246,767-56,252,877 OR4D2
    nsv6520815copy number variation1nstd223human GRCh38 chr17: 58,170,247-58,180,898 , GRCh37.p13 chr17: 56,247,608-56,258,259 OR4D2
    nsv5026639copy number variation1nstd200human GRCh38 chr17: 58,170,247-58,180,898 , GRCh37.p13 chr17: 56,247,608-56,258,259 OR4D2
    nsv5026640copy number variation1nstd200human GRCh38 chr17: 58,171,053-58,172,170 , GRCh37.p13 chr17: 56,248,414-56,249,531 OR4D2
    esv995666copy number variation1estd180human NCBI36 chr17: 53,600,710-53,601,233 , GRCh37.p13 chr17: 56,245,711-56,246,234 , GRCh38.p12 chr17: 58,168,350-58,168,873 OR4D2
    esv1962204copy number variation1estd194human NCBI36 chr17: 53,601,375-53,601,376 , GRCh37.p13 chr17: 56,246,376-56,246,377 , GRCh38.p12 chr17: 58,169,015-58,169,016 OR4D2
    nsv4576325mobile element insertion1nstd166human GRCh37.p13 chr17: 56,246,326-56,246,326 , GRCh38.p12 chr17: 58,168,965-58,168,965 OR4D2
    nsv6577817inversion1nstd223human GRCh38 chr17: 58,167,859-58,168,186 , GRCh37.p13 chr17: 56,245,220-56,245,547 OR4D2
    nsv6984115copy number variation1nstd229human GRCh38 chr17: 58,145,642-58,171,230 , GRCh37.p13 chr17: 56,223,003-56,248,591 MSX2P1, OR4D1, 1 more genes
    nsv3160070copy number variation1nstd151human GRCh37 chr17: 56,232,512-56,247,945 , GRCh38.p12 chr17: 58,155,151-58,170,584 OR4D1, MSX2P1, 1 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 PRPSAP1, CACNG1, 1350 more genes
    nsv3914957copy number variation1nstd102humanPathogenic GRCh37 chr17: 55,496,167-57,812,825 , GRCh38 chr17: 57,418,806-59,735,464 , NCBI36 chr17: 52,851,166-55,167,607 CLTC, LOC101927557, 67 more genes
    nsv6634423copy number variation1nstd102humanPathogenic GRCh37 chr17: 55,043,662-56,728,123 , GRCh38.p12 chr17: 56,966,301-58,650,762 RNU7-134P, DYNLL2-DT, 42 more genes
    nsv3917224copy number variation1nstd102humanPathogenic GRCh38 chr17: 56,958,745-58,171,125 , NCBI36 chr17: 52,391,105-53,603,485 , GRCh37 chr17: 55,036,106-56,248,486 MRPS23, MSX2P1, 24 more genes
    nsv7098791copy number variation1nstd102humanPathogenic GRCh37 chr17: 55,442,363-56,309,063 , GRCh38.p12 chr17: 57,365,002-58,231,702 MKS1, OR4D2, 21 more genes
    nsv7098766copy number variation1nstd102humanPathogenic GRCh37 chr17: 55,806,534-56,540,597 , GRCh38.p12 chr17: 57,729,173-58,463,236 SRSF1, LOC105371840, 24 more genes
    nsv3903684copy number variation1nstd102humanPathogenic GRCh37 chr17: 8,547-81,060,040 , GRCh38.p12 chr17: 158,756-83,102,004 MIR3185, YWHAEP6, 2366 more genes
    nsv3899740copy number variation1nstd102humanPathogenic GRCh37 chr17: 7,214-81,058,310 , GRCh38.p12 chr17: 157,423-83,100,564 P4HB, LOC105371808, 2366 more genes
    nsv3906245copy number variation1nstd102humanPathogenic GRCh37 chr17: 12,344-81,057,996 , GRCh38.p12 chr17: 162,553-83,100,251 MIR21, LOC105371899, 2366 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
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