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Items: 1 to 20 of 154

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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
    nsv4330632inversion1nstd166human GRCh37.p13 chr17: 18,838,526-72,042,289 , GRCh38.p12 chr17: 18,935,213-74,046,150 , ACACA, 1499 more genes
    nsv3920056copy number variation1nstd102humanUncertain significance NCBI36 chr17: 43,882,989-44,985,282 , GRCh38 chr17: 48,450,628-49,552,921 , GRCh37 chr17: 46,527,990-47,630,283 ZNF652-AS1, RPS10P25, 55 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
    nsv3913486copy number variation1nstd102humanPathogenic GRCh38 chr17: 48,520,885-49,511,208 , NCBI36 chr17: 43,953,246-44,943,569 , GRCh37 chr17: 46,598,247-47,588,570 MIR6165, NGFR, 54 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
    nsv3911757copy number variation1nstd102humanPathogenic NCBI36 chr17: 43,419,251-44,761,758 , GRCh37 chr17: 46,064,252-47,406,759 , GRCh38 chr17: 47,986,886-49,329,397 LINC02086, RNU6-1152P, 59 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
    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
    nsv3890215copy number variation1nstd102humanLikely pathogenic GRCh37 chr17: 46,481,089-51,396,368 , GRCh38.p12 chr17: 48,403,727-53,319,007 ATP5MC1, CHAD, 124 more genes
    nsv3161888copy number variation1nstd151human GRCh37 chr17: 46,627,693-46,700,502 , GRCh38.p12 chr17: 48,550,331-48,623,140 HOXB6, MIR10A, 8 more genes
    esv4010354copy number variation1estd233human GRCh37 chr17: 46,556,000-46,886,000 , GRCh38.p12 chr17: 48,478,638-48,808,638 COX6B1P2, HOXB1, 24 more genes
    nsv1878568short tandem repeat1nstd128human GRCh37 chr17: 46,655,990-46,656,011 , GRCh38.p12 chr17: 48,578,628-48,578,649 HOXB4, HOXB3, 1 more genes
    nsv1877987short tandem repeat3nstd128human GRCh37 chr17: 46,655,910-46,655,925 , GRCh38.p12 chr17: 48,578,548-48,578,563 MIR10A, HOXB3, 1 more genes
    esv3901451copy number variation1estd225human GRCh37 chr17: 46,639,703-46,713,928 , GRCh38.p12 chr17: 48,562,341-48,636,566 HOXB3, HOXB4, 9 more genes
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