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Items: 1 to 20 of 183

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148092copy number variation1nstd102humanPathogenic GRCh37 chr15: 75,165,490-102,520,892 , GRCh38.p12 chr15: 74,873,149-101,980,689 RPL9P8, COMMD4P1, 547 more genes
    nsv7098892copy number variation1nstd102humanPathogenic GRCh37 chr15: 84,228,005-102,264,590 , GRCh38.p12 chr15: 83,559,253-101,724,387 CIB1, RPS12P26, 326 more genes
    nsv6977574copy number variation1nstd229human GRCh38 chr15: 92,198,670-92,502,215 , GRCh37.p13 chr15: 92,741,900-93,045,445 C15orf32, ST8SIA2, 5 more genes
    nsv6972662copy number variation1nstd229human GRCh38 chr15: 92,426,984-92,533,463 , GRCh37.p13 chr15: 92,970,214-93,076,693 LOC104613533, C15orf32, 1 more genes
    nsv6972104copy number variation1nstd229human GRCh38 chr15: 92,476,683-92,479,196 , GRCh37.p13 chr15: 93,019,913-93,022,426 C15orf32
    nsv6970599copy number variation1nstd229human GRCh38 chr15: 92,217,541-92,557,565 , GRCh37.p13 chr15: 92,760,771-93,100,795 ST8SIA2, C15orf32, 5 more genes
    nsv6965127copy number variation1nstd229human GRCh38 chr15: 92,429,903-92,578,172 , GRCh37.p13 chr15: 92,973,133-93,121,402 ST8SIA2, C15orf32, 2 more genes
    nsv6964272copy number variation1nstd229human GRCh38 chr15: 92,495,961-92,496,166 , GRCh37.p13 chr15: 93,039,191-93,039,396 C15orf32
    nsv6963474copy number variation1nstd229human GRCh38 chr15: 92,497,152-92,504,541 , GRCh37.p13 chr15: 93,040,382-93,047,771 C15orf32
    nsv6962360copy number variation1nstd229human GRCh38 chr15: 92,484,855-92,494,897 , GRCh37.p13 chr15: 93,028,085-93,038,127 C15orf32
    nsv6637683copy number variation1nstd102humanPathogenic GRCh37 chr15: 77,512,817-102,035,027 , GRCh38.p12 chr15: 77,220,475-101,494,824 LINC02253, LOC107984790, 463 more genes
    nsv6583445inversion1nstd223human GRCh38 chr15: 92,476,938-92,481,944 , GRCh37.p13 chr15: 93,020,168-93,025,174 C15orf32
    nsv6511826copy number variation1nstd223human GRCh38 chr15: 92,497,152-92,504,539 , GRCh37.p13 chr15: 93,040,382-93,047,769 C15orf32
    nsv6505159copy number variation1nstd223human GRCh38 chr15: 92,476,683-92,479,193 , GRCh37.p13 chr15: 93,019,913-93,022,423 C15orf32
    nsv6502480copy number variation1nstd223human GRCh38 chr15: 92,217,541-92,557,558 , GRCh37.p13 chr15: 92,760,771-93,100,788 NPM1P5, ST8SIA2, 5 more genes
    nsv6497538copy number variation1nstd223human GRCh38 chr15: 92,487,988-92,488,593 , GRCh37.p13 chr15: 93,031,218-93,031,823 C15orf32
    nsv6495817copy number variation1nstd223human GRCh38 chr15: 92,479,758-92,480,221 , GRCh37.p13 chr15: 93,022,988-93,023,451 C15orf32
    nsv6291795copy number variation1nstd102humanPathogenic GRCh37 chr15: 89,520,451-93,926,491 , GRCh38.p12 chr15: 88,977,220-93,383,262 LINC00930, TRY-GTA12-1, 106 more genes
    nsv6290316copy number variation1nstd102humanPathogenic GRCh37 chr15: 88,465,861-94,411,846 , GRCh38.p12 chr15: 87,922,630-93,868,617 LOC105370964, MRPL46, 130 more genes
    nsv6288567insertion1nstd214human GRCh38 chr15: 92,479,978-92,479,978 , GRCh37.p13 chr15: 93,023,208-93,023,208 C15orf32
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