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Items: 1 to 20 of 168

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5937790copy number variation1nstd209human GRCh38 chr17: 30,668,045-32,084,125 , GRCh37.p13 chr17: 28,995,063-30,411,144 , OMG, 39 more genes
    nsv5016007copy number variation1nstd200human GRCh38 chr17: 31,557,605-31,559,132 , GRCh37.p13 chr17: 29,884,624-29,886,151 MIR193A
    nsv5016006copy number variation1nstd200human GRCh38 chr17: 31,555,979-31,560,380 , GRCh37.p13 chr17: 29,882,998-29,887,399 MIR193A
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4729791copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,039,844-30,412,788 , GRCh38.p12 chr17: 30,712,826-32,085,769 ADAP2, TEFM, 37 more genes
    nsv4684241copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,393,104-30,427,403 , GRCh38.p12 chr17: 31,066,086-32,100,384 LOC102724625, RNA5SP437, 26 more genes
    nsv4680260copy number variation1nstd189human GRCh37.p13 chr17: 29,540,484-30,103,257 , GRCh38.p12 chr17: 31,213,466-31,776,238 AK4P1, EVI2A, 16 more genes
    nsv4675286copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,088,218-30,159,137 , GRCh38.p12 chr17: 30,761,200-31,832,118 CRLF3, RN7SL45P, 30 more genes
    nsv4675209copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,373,189-30,412,788 , GRCh38.p12 chr17: 31,046,171-32,085,769 GPR160P2, MIR4724, 27 more genes
    nsv4674861copy number variation1nstd102humanLikely benign GRCh37 chr17: 29,883,686-29,972,827 , GRCh38.p12 chr17: 31,556,667-31,645,808 MIR365B, RNU6ATAC7P, 2 more genes
    nsv4578269copy number variation1nstd102humanPathogenic GRCh37 chr17: 28,941,066-30,326,958 , GRCh38.p12 chr17: 30,614,048-31,999,939 LOC105371723, MIR4724, 41 more genes
    nsv4457831copy number variation1nstd102humanPathogenic GRCh37 chr17: 21,690,653-38,772,647 , GRCh38.p12 chr17: 22,164,047-40,616,395 LOC105371753, TAOK1, 474 more genes
    nsv4457704copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,054,315-30,409,336 , GRCh38.p12 chr17: 30,727,297-32,082,317 SH3GL1P1, LOC646030, 36 more genes
    nsv4457460copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,054,315-30,391,711 , GRCh38.p12 chr17: 30,727,297-32,064,692 LOC107984974, MIR4733, 36 more genes
    nsv4457440copy number variation1nstd102humanPathogenic GRCh37 chr17: 28,999,903-30,409,337 , GRCh38.p12 chr17: 30,672,885-32,082,318 MIR365B, RNU6ATAC7P, 38 more genes
    nsv4384972copy number variation1nstd173human GRCh37 chr17: 27,710,978-33,392,085 , GRCh38.p12 chr17: 29,383,960-35,065,066 , LOC105371737, 137 more genes
    nsv4365362copy number variation1nstd173human GRCh37 chr17: 28,997,866-30,391,813 , GRCh38.p12 chr17: 30,670,848-32,064,794 , RN7SL79P, 39 more genes
    nsv4349272copy number variation1nstd102humanPathogenic GRCh37 chr17: 29,111,368-30,183,819 , GRCh38.p12 chr17: 30,784,350-31,856,800 ADAP2, EVI2A, 31 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
    nsv4236585copy number variation1nstd166human GRCh37.p13 chr17: 29,873,479-29,886,304 , GRCh38.p12 chr17: 31,546,460-31,559,285 MIR193A, TRT-CGT4-1
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