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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
    nsv5554090sequence alteration1nstd206human GRCh38 chr17: 32,109,732-67,925,723 , GRCh37.p13 chr17: 30,436,751-65,921,839 , APOH, 1099 more genes
    nsv5151108mobile element insertion1nstd203human GRCh38 chr17: 58,336,446-58,336,456 , GRCh37.p13 chr17: 56,413,807-56,413,817 TSPOAP1-AS1, MIR4736
    nsv4432554copy number variation1nstd172human GRCh37.p13 chr17: 56,402,001-56,423,000 , GRCh38.p12 chr17: 58,324,640-58,345,639 SUPT4H1, TSPOAP1, 3 more genes
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv4272058copy number variation1nstd166human GRCh37.p13 chr17: 56,411,354-56,411,414 , GRCh38.p12 chr17: 58,333,993-58,334,053 MIR4736, TSPOAP1-AS1
    nsv4253010copy number variation1nstd166human GRCh37.p13 chr17: 56,411,359-56,411,463 , GRCh38.p12 chr17: 58,333,998-58,334,102 MIR4736, TSPOAP1-AS1
    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
    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 LOC105371922, GJD3, 1855 more genes
    nsv3913552copy number variation1nstd102humanPathogenic GRCh38 chr17: 36,449,220-75,053,130 , NCBI36 chr17: 54,950,518-70,560,820 , GRCh37 chr17: 57,595,736-73,049,225 RNU6-131P, ZNF652, 1075 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
    nsv3911563copy number variation1nstd102humanPathogenic NCBI36 chr17: 45,918,236-63,677,950 , GRCh37 chr17: 48,563,237-65,936,105 , GRCh38 chr17: 36,449,220-68,170,214 PLEKHH3, CHCT1, 958 more genes
    nsv3909511copy number variation1nstd102humanPathogenic GRCh37 chr17: 42,580,684-81,085,615 , GRCh38.p12 chr17: 44,503,316-83,137,846 FOXK2, SOCS3-DT, 958 more genes
    nsv3907261copy number variation2nstd102humanPathogenic GRCh37 chr17: 526-81,041,938 , GRCh38.p12 chr17: 150,733-83,084,062 SMURF2, LOC112268199, 2366 more genes
    nsv3906711copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 55,916,829-56,770,618 , GRCh38.p12 chr17: 57,839,468-58,693,257 LPO, MPO, 34 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
    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
    nsv3895703copy number variation1nstd102humanPathogenic GRCh37 chr17: 56,321,134-62,080,001 , GRCh38.p12 chr17: 58,243,773-64,002,641 GH2, LOC105371847, 161 more genes
    nsv3892374copy number variation1nstd102humanPathogenic GRCh37 chr17: 52,189,051-57,477,162 , GRCh38.p12 chr17: 54,111,690-59,399,801 RN7SKP14, RNU6-1249P, 93 more genes
    nsv3890268copy number variation1nstd102humanPathogenic GRCh37 chr17: 49,076,980-58,740,945 , GRCh38.p12 chr17: 50,999,619-60,663,584 NDUFB8P2, LPO, 161 more genes
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