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Items: 1 to 20 of 120

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5967628inversion1nstd209human GRCh37.p13 chr17: 75,065,062-75,092,554 , GRCh38 chr17: 77,068,980-77,096,472 SEC14L1, SNHG20, 2 more genes
    nsv5559991sequence alteration1nstd206human GRCh38 chr17: 77,068,981-77,096,473 , GRCh37.p13 chr17: 75,065,063-75,092,555 SEC14L1, SNHG20, 2 more genes
    nsv5523938copy number variation1nstd206human GRCh38 chr17: 77,055,249-77,181,065 , GRCh37.p13 chr17: 75,051,331-75,177,147 , SEC14L1, 5 more genes
    nsv5016795copy number variation1nstd200human GRCh38 chr17: 77,085,475-77,091,159 , GRCh37.p13 chr17: 75,081,557-75,087,241 SEC14L1, SCARNA16, 2 more genes
    nsv5016794copy number variation1nstd200human GRCh38 chr17: 77,085,408-77,088,534 , GRCh37.p13 chr17: 75,081,490-75,084,616 SCARNA16, MIR6516, 2 more genes
    nsv4859064copy number variation1nstd200human GRCh37 chr17: 75,081,592-75,090,646 , GRCh38.p12 chr17: 77,085,510-77,094,564 MIR6516, SEC14L1, 2 more genes
    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
    nsv4457730copy number variation1nstd102humanUncertain significance GRCh37 chr17: 75,050,166-75,094,971 , GRCh38.p12 chr17: 77,054,084-77,098,889 SNHG20, MIR6516, 2 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
    nsv4265271copy number variation1nstd166human GRCh37.p13 chr17: 75,025,057-75,099,776 , GRCh38.p12 chr17: 77,028,975-77,103,694 SEC14L1, SNHG20, 2 more genes
    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
    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
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