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Items: 1 to 20 of 139

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7095479copy number variation1nstd102humanUncertain significance GRCh37 chr19: 38,375,572-39,738,787 , GRCh38.p12 chr19: 37,884,932-39,248,147 HNRNPL, RN7SL663P, 45 more genes
    nsv7016814copy number variation1nstd229human GRCh38 chr19: 38,329,827-38,329,922 , GRCh37.p13 chr19: 38,820,467-38,820,562 KCNK6
    nsv7014368copy number variation1nstd229human GRCh38 chr19: 38,328,845-38,328,899 , GRCh37.p13 chr19: 38,819,485-38,819,539 KCNK6
    nsv7008156copy number variation1nstd229human GRCh38 chr19: 36,851,242-46,031,790 , GRCh37.p13 chr19: 37,342,144-46,535,048 LOC105372390, LOC107985291, 396 more genes
    nsv7005713copy number variation1nstd229human GRCh38 chr19: 33,458,650-39,721,746 , GRCh37.p13 chr19: 33,949,556-40,212,386 , TYROBP, 259 more genes
    nsv6529884copy number variation1nstd223human GRCh38 chr19: 38,331,678-38,332,901 , GRCh37.p13 chr19: 38,822,318-38,823,541 KCNK6
    nsv6528802copy number variation1nstd223human GRCh38 chr19: 37,602,649-38,484,499 , GRCh37.p13 chr19: 38,093,550-38,975,139 SPRED3, PSMD8, 30 more genes
    nsv6522253copy number variation1nstd223human GRCh38 chr19: 38,297,603-38,318,193 , GRCh37.p13 chr19: 38,788,243-38,808,833 YIF1B, C19orf33, 1 more genes
    nsv6515767copy number variation1nstd223human GRCh38 chr19: 38,276,054-38,323,179 , GRCh37.p13 chr19: 38,766,694-38,813,819 YIF1B, KCNK6, 2 more genes
    nsv6290300copy number variation1nstd102humanPathogenic GRCh37 chr19: 19,546,923-41,313,229 , GRCh38.p12 chr19: 19,436,114-40,807,324 ZNF420, LOC105372330, 574 more genes
    nsv6133523copy number variation1nstd213human GRCh37 chr19: 34,000,000-42,200,001 , GRCh38.p12 chr19: 33,509,094-41,696,083 , ACTN4, 345 more genes
    nsv6104821insertion1nstd212human GRCh38 chr19: 38,328,889-38,328,889 , GRCh37.p13 chr19: 38,819,529-38,819,529 KCNK6
    nsv5975145insertion1nstd209human GRCh38 chr19: 38,328,878-38,328,878 , GRCh37.p13 chr19: 38,819,518-38,819,518 KCNK6
    nsv5556604sequence alteration1nstd206human GRCh38 chr19: 38,269,810-38,604,627 , GRCh37.p13 chr19: 38,760,450-39,095,267 , PSMD8, 12 more genes
    nsv5027872copy number variation1nstd200human GRCh38 chr19: 38,331,681-38,332,901 , GRCh37.p13 chr19: 38,822,321-38,823,541 KCNK6
    nsv4676223copy number variation1nstd102humanUncertain significance GRCh37 chr19: 38,512,717-39,291,526 , GRCh38.p12 chr19: 38,022,077-38,800,886 MAP4K1-AS1, LGALS7B, 25 more genes
    nsv4457372copy number variation1nstd102humanPathogenic GRCh37 chr19: 28,271,106-49,213,832 , GRCh38.p12 chr19: 27,780,198-48,710,575 ZNF461, LOC101927572, 735 more genes
    nsv4265654copy number variation1nstd166human GRCh37.p13 chr19: 38,819,794-38,842,187 , GRCh38.p12 chr19: 38,329,154-38,351,547 KCNK6, CATSPERG
    nsv3913730copy number variation1nstd102humanPathogenic NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354 BCKDHA, ADGRE5, 1102 more genes
    nsv3912447copy number variation1nstd102humanPathogenic NCBI36 chr19: 42,502,119-47,934,680 , GRCh37 chr19: 37,810,279-43,242,840 , GRCh38 chr19: 37,319,377-42,738,688 MIR8077, TRI-TAT1-1, 233 more genes
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