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Items: 1 to 20 of 961

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147062copy number variation1nstd232human GRCh37.p13 chrX: 1,562,146-1,562,281 , GRCh38.p12 chrX: 1,443,253-1,443,388 ASMTL
    nsv7141285copy number variation1nstd232human GRCh37.p13 chrX: 1,524,136-1,524,202 , GRCh38.p12 chrX: 1,405,243-1,405,309 ASMTL, ASMTL-AS1
    nsv7140814copy number variation1nstd232human GRCh37.p13 chrX: 1,521,560-1,521,610 , GRCh38.p12 chrX: 1,402,667-1,402,717 ASMTL, ASMTL-AS1
    nsv7137063copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-155,240,074 , GRCh38.p12 chrX: 284,188-156,010,409 RN7SL581P, HMGB1P32, 2151 more genes
    nsv7098867copy number variation1nstd102humanPathogenic GRCh37 chrX: 200,855-6,069,814 , GRCh38.p12 chrX: 284,188-6,151,773 RPL14P5, NLGN4X, 64 more genes
    nsv6636182copy number variation1nstd102humanUncertain significance GRCh37 chrX: 1,211,466-2,140,595 , GRCh38.p12 chrX: 1,111,313-2,222,554 SLC25A6, ASMTL, 17 more genes
    nsv6636179copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,547-1,536,716 , GRCh38.p12 chrX: 251,880-1,417,823 LOC100418703, PLCXD1, 19 more genes
    nsv6636141copy number variation1nstd102humanUncertain significance GRCh37 chrX: 1,324,509-1,805,618 , GRCh38.p12 chrX: 1,205,616-1,686,725 IL3RA, LOC101928032, 11 more genes
    nsv6636130copy number variation1nstd102humanUncertain significance GRCh37 chrX: 852,805-1,717,093 , GRCh38.p12 chrX: 892,070-1,598,200 RPL14P5, ASMTL, 14 more genes
    nsv6636125copy number variation1nstd102humanUncertain significance GRCh37 chrX: 1,561,584-1,890,883 , GRCh38.p12 chrX: 1,442,691-1,771,990 ASMT, LINC02968, 4 more genes
    nsv6636109copy number variation1nstd102humanUncertain significance GRCh37 chrX: 1,240,319-1,605,584 , GRCh38.p12 chrX: 1,140,166-1,486,691 IL3RA, LOC101928032, 10 more genes
    nsv6636090copy number variation1nstd102humanPathogenic GRCh37 chrX: 201,705-2,696,762 , GRCh38.p12 chrX: 285,038-2,778,721 ASMT, LINC00685, 33 more genes
    nsv6636081copy number variation1nstd102humanUncertain significance GRCh37 chrX: 1,262,175-1,624,748 , GRCh38.p12 chrX: 1,162,022-1,505,855 MIR3690, LOC652608, 10 more genes
    nsv6635065copy number variation1nstd227human GRCh37 chrX: 976,585-1,537,415 , GRCh38.p12 chrX: 1,015,850-1,418,522 , SLC25A6, 11 more genes
    nsv6634242copy number variation1nstd224human GRCh37 chrX: 1-155,270,560 , GRCh38.p12 chrX: 10,001-156,030,895 NR0B1, ALAS2, 2154 more genes
    nsv6634094copy number variation4nstd224human GRCh37 chrY: 1-59,373,566 , GRCh38.p12 chrY: 10,001-57,217,415 ASMT, ASS1P6, 570 more genes
    nsv6315577complex substitution1nstd102humanPathogenic GRCh37 chrX: 590,376-56,315,041 , GRCh38.p12 chrX: 629,641-56,288,608 ACTG1P10, NR0B1, 778 more genes
    nsv6315454copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-10,368,820 , GRCh38.p12 chrX: 251,879-10,400,780 LOC107985675, PRKX-AS1, 101 more genes
    nsv6315430copy number variation1nstd102humanPathogenic GRCh37 chrX: 168,546-11,080,743 , GRCh38.p12 chrX: 251,879-11,062,623 RPS27AP20, PPP2R3B, 103 more genes
    nsv6315393copy number variation1nstd102humanPathogenic GRCh37 chrX: 61,545-155,226,048 , GRCh38.p12 chrX: 11,545-155,996,383 H2BP8, LOC101060199, 2151 more genes
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