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Items: 1 to 20 of 146

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5933388copy number variation1nstd209human GRCh38 chr17: 30,221,446-30,221,495 , GRCh37.p13 chr17: 28,548,464-28,548,513 , SLC6A4
    nsv5873021copy number variation1nstd209human GRCh38 chr17: 30,200,787-30,202,786 , GRCh37.p13 chr17: 28,527,805-28,529,804 SLC6A4
    nsv5521229copy number variation1nstd206human GRCh38 chr17: 30,187,051-30,193,077 , GRCh37.p13 chr17: 28,514,069-28,520,095 SLC6A4
    nsv5516318copy number variation1nstd206human GRCh38 chr17: 30,181,943-30,206,859 , GRCh37.p13 chr17: 28,508,961-28,533,877 SLC6A4, NSRP1
    nsv5358791translocation1nstd200human GRCh38 chr17: 30,226,743-30,226,743 , GRCh38 chr17: 30,226,655-30,226,655 , GRCh37.p13 chr17: 28,553,673-28,553,673 , GRCh37.p13 chr17: 28,553,761-28,553,761 SLC6A4
    nsv5149187mobile element insertion1nstd203human GRCh38 chr17: 30,213,647-30,213,659 , GRCh37.p13 chr17: 28,540,665-28,540,677 , SLC6A4
    nsv5144873mobile element insertion1nstd203human GRCh38 chr17: 30,220,489-30,220,505 , GRCh37.p13 chr17: 28,547,507-28,547,523 , SLC6A4
    nsv5023933copy number variation1nstd200human GRCh38 chr17: 30,234,927-30,320,783 , GRCh37.p13 chr17: 28,561,945-28,647,801 TMIGD1, RNU6-1267P, 4 more genes
    nsv5023932copy number variation1nstd200human GRCh38 chr17: 30,180,103-30,210,437 , GRCh37.p13 chr17: 28,507,121-28,537,455 SLC6A4, NSRP1
    nsv5010313copy number variation1nstd200human GRCh38 chr17: 30,235,193-30,239,450 , GRCh37.p13 chr17: 28,562,211-28,566,468 LOC105371720, SLC6A4
    nsv4864601copy number variation1nstd200human GRCh37 chr17: 28,561,945-28,647,801 , GRCh38.p12 chr17: 30,234,927-30,320,783 TMIGD1, LOC105371720, 4 more genes
    nsv4762422inversion1nstd199human GRCh37 chr17: 151-36,202,676 , GRCh38.p12 chr17: 150,358-36,446,544 , ABR, 1046 more genes
    nsv4575254mobile element insertion1nstd166human GRCh37.p13 chr17: 28,523,309-28,523,309 , GRCh38.p12 chr17: 30,196,291-30,196,291 SLC6A4
    nsv4574117mobile element insertion1nstd166human GRCh37.p13 chr17: 28,523,301-28,523,301 , GRCh38.p12 chr17: 30,196,283-30,196,283 SLC6A4
    nsv4531956copy number variation1nstd166human GRCh37.p13 chr17: 28,523,999-28,548,000 , GRCh38.p12 chr17: 30,196,981-30,220,982 , SLC6A4
    nsv4504248mobile element insertion1nstd166human GRCh37.p13 chr17: 28,521,083-28,521,083 , GRCh38.p12 chr17: 30,194,065-30,194,065 SLC6A4
    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
    nsv4384972copy number variation1nstd173human GRCh37 chr17: 27,710,978-33,392,085 , GRCh38.p12 chr17: 29,383,960-35,065,066 , LOC105371737, 137 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
    nsv4249129copy number variation1nstd166human GRCh37.p13 chr17: 28,548,430-28,548,501 , GRCh38.p12 chr17: 30,221,412-30,221,483 , SLC6A4
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