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Items: 1 to 20 of 114

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4676341copy number variation1nstd102humanUncertain significance GRCh37 chr17: 74,509,193-75,602,123 , GRCh38.p12 chr17: 76,513,111-77,606,041 CYCSP40, RNU6-97P, 38 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
    nsv4457646copy number variation1nstd102humanPathogenic GRCh37 chr17: 62,778,720-81,041,938 , GRCh38.p12 chr17: 64,782,602-83,084,062 LOC107985089, ARSG, 448 more genes
    nsv3962324insertion1nstd168human GRCh38 chr17: 77,178,982-77,248,009 , GRCh37.p13 chr17: 75,175,064-75,244,091 CYCSP40, SEC14L1
    nsv3919156copy number variation1nstd102humanPathogenic GRCh38 chr17: 69,916,435-83,102,552 , GRCh37 chr17: 67,912,576-81,048,189 , NCBI36 chr17: 65,424,171-78,653,717 CD300A, RNF213, 359 more genes
    nsv3917654copy number variation1nstd102humanPathogenic NCBI36 chr17: 64,716,815-78,637,842 , GRCh37 chr17: 67,205,220-81,044,553 , GRCh38 chr17: 69,209,079-83,086,677 LOC101928447, GRB2, 368 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
    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
    nsv3909523copy number variation1nstd102humanPathogenic GRCh37 chr17: 63,689,671-81,041,938 , GRCh38.p12 chr17: 65,693,553-83,084,062 RPL38, RNF157-AS1, 428 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
    nsv3907721copy number variation1nstd102humanUncertain significance GRCh37 chr17: 75,104,943-75,602,123 , GRCh38.p12 chr17: 77,108,861-77,606,041 LOC400622, LOC100507351, 11 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
    nsv3906075copy number variation1nstd102humanPathogenic GRCh37 chr17: 67,002,415-81,041,938 , GRCh38.p12 chr17: 69,006,274-83,084,062 CEP131, RPTOR, 374 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
    nsv3897835copy number variation1nstd102humanPathogenic GRCh37 chr17: 73,951,701-81,041,938 , GRCh38.p12 chr17: 75,955,620-83,084,062 ARHGDIA, CCDC137, 230 more genes
    esv4010450copy number variation1estd233human GRCh37 chr17: 74,666,000-77,991,000 , GRCh38.p12 chr17: 76,669,918-80,017,201 , BIRC5, 88 more genes
    nsv1899753short tandem repeat7nstd128human GRCh37 chr17: 75,194,659-75,194,674 , GRCh38.p12 chr17: 77,198,577-77,198,592 SEC14L1, CYCSP40
    nsv1896857short tandem repeat3nstd128human GRCh37 chr17: 75,193,700-75,193,712 , GRCh38.p12 chr17: 77,197,618-77,197,630 SEC14L1, CYCSP40
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