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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5974581inversion1nstd209human GRCh38 chr5: 72,480,203-72,490,776 , GRCh37.p13 chr5: 71,776,030-71,786,603 ZNF366
    nsv5555006sequence alteration1nstd206human GRCh38 chr5: 72,491,129-72,491,129 , GRCh37.p13 chr5: 71,786,956-71,786,956 ZNF366
    nsv5536013insertion1nstd206human GRCh38 chr5: 72,491,124-72,491,124 , GRCh37.p13 chr5: 71,786,951-71,786,951 ZNF366
    nsv5368516translocation1nstd200human GRCh38 chr5: 72,504,785-72,504,785 , GRCh38 chr5: 72,504,223-72,504,223 , GRCh37.p13 chr5: 71,800,050-71,800,050 , GRCh37.p13 chr5: 71,800,612-71,800,612 ZNF366
    nsv5344542translocation1nstd200human GRCh37 chr5: 71,800,050-71,800,050 , GRCh37 chr5: 71,800,612-71,800,612 , GRCh38.p12 chr5: 72,504,223-72,504,223 , GRCh38.p12 chr5: 72,504,785-72,504,785 ZNF366
    nsv5328637translocation1nstd204human GRCh38.p13 chr5: 72,504,223-72,504,223 , GRCh38.p13 chr5: 72,504,785-72,504,785 , GRCh37.p13 chr5: 71,800,050-71,800,050 , GRCh37.p13 chr5: 71,800,612-71,800,612 ZNF366
    nsv4937771copy number variation1nstd200human GRCh38 chr5: 72,487,848-72,494,000 , GRCh37.p13 chr5: 71,783,675-71,789,827 ZNF366
    nsv4729291copy number variation1nstd102humanUncertain significance GRCh37 chr5: 71,017,577-72,056,514 , GRCh38.p12 chr5: 71,721,750-72,760,687 RN7SL153P, MRPS27, 14 more genes
    nsv4578696copy number variation1nstd102humanLikely pathogenic GRCh38 chr5: 58,780,641-73,523,380 , GRCh37.p13 chr5: 58,076,468-72,819,205 TRIM23, BTF3, 215 more genes
    nsv4455596copy number variation2nstd102humanUncertain significance GRCh37 chr5: 71,721,970-72,431,813 , GRCh38.p12 chr5: 72,426,143-73,135,986 TMEM171, RPL7P22, 10 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RNU1-150P, RNU6-727P, 1757 more genes
    nsv4391931copy number variation1nstd171human GRCh37 chr5: 71,774,097-71,774,136 , GRCh38.p12 chr5: 72,478,270-72,478,309 ZNF366
    nsv4126922copy number variation1nstd166human GRCh37.p13 chr5: 71,800,050-71,800,612 , GRCh38.p12 chr5: 72,504,223-72,504,785 ZNF366
    nsv3960441copy number variation1nstd168human GRCh38 chr5: 72,479,035-72,498,857 , GRCh37.p13 chr5: 71,774,862-71,794,684 ZNF366
    nsv3914679copy number variation1nstd102humanUncertain significance GRCh38 chr5: 71,915,937-72,562,961 , GRCh37 chr5: 71,211,764-71,858,788 , NCBI36 chr5: 71,247,520-71,894,544 LOC105379028, MIR4803, 10 more genes
    nsv3912593copy number variation1nstd102humanUncertain significance NCBI36 chr5: 332,389-180,837,866 , GRCh37.p13 chr5: 279,389-180,905,260 , GRCh38.p12 chr5: 279,274-181,478,259 LOC105378993, LOC107986375, 2492 more genes
    nsv3911585copy number variation1nstd102humanPathogenic NCBI36 chr5: 75,149-73,744,306 , GRCh38 chr5: 22,149-74,412,725 , GRCh37 chr5: 22,149-73,708,550 LINC02241, ATPSCKMT, 878 more genes
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 MEGF10, LOC100128407, 2080 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 LOC105374618, HARS1, 2499 more genes
    nsv3884207copy number variation1nstd102humanLikely benign GRCh37 chr5: 71,450,015-72,008,955 , GRCh38.p12 chr5: 72,154,188-72,713,128 RPL10AP8, RN7SL153P, 8 more genes
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