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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4948811copy number variation1nstd200human GRCh38 chr5: 61,159,096-61,159,463 , GRCh37.p13 chr5: 60,454,923-60,455,290 SMIM15
    nsv4948808copy number variation1nstd200human GRCh38 chr5: 60,809,384-61,514,334 , GRCh37.p13 chr5: 60,105,211-60,810,161 LOC105378994, ERCC8-AS1, 12 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
    nsv4456752copy number variation2nstd102humanUncertain significance GRCh37 chr5: 60,101,557-60,658,345 , GRCh38.p12 chr5: 60,805,730-61,362,518 LINC02057, LOC100421309, 10 more genes
    nsv4456549copy number variation1nstd102humanUncertain significance GRCh37 chr5: 60,101,557-60,809,784 , GRCh38.p12 chr5: 60,805,730-61,513,957 LOC100421561, NDUFAF2, 12 more genes
    nsv4456135copy number variation1nstd102humanUncertain significance GRCh37 chr5: 60,116,532-60,809,784 , GRCh38.p12 chr5: 60,820,705-61,513,957 ELOVL7, ERCC8, 12 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
    nsv4337631sequence alteration1nstd166human GRCh37.p13 chr5: 59,960,463-64,048,177 , GRCh38.p12 chr5: 60,664,636-64,752,350 , ERCC8, 46 more genes
    nsv4125552copy number variation1nstd166human GRCh37.p13 chr5: 60,332,966-60,462,608 , GRCh38.p12 chr5: 61,037,139-61,166,781 SMIM15-AS1, NDUFAF2, 1 more genes
    nsv4119813copy number variation1nstd166human GRCh37.p13 chr5: 39,131,458-67,637,618 , GRCh38.p12 chr5: 39,131,356-68,341,790 , ESM1, 305 more genes
    nsv3923429copy number variation1nstd102humanPathogenic GRCh37 chr5: 49,584,189-62,445,597 , NCBI36 chr5: 49,619,946-62,481,353 , GRCh38 chr5: 50,288,355-63,149,770 ISCA1P1, LOC643307, 163 more genes
    nsv3920391copy number variation1nstd102humanPathogenic GRCh38 chr5: 35,201,559-61,903,141 , GRCh37 chr5: 35,201,661-61,198,968 , NCBI36 chr5: 35,237,418-61,234,725 KRT18P56, LINC01265, 290 more genes
    nsv3919086copy number variation1nstd102humanPathogenic NCBI36 chr5: 59,830,661-63,259,366 , GRCh38 chr5: 60,499,077-63,927,783 , GRCh37 chr5: 59,794,904-63,223,610 LOC105378999, DEPDC1B, 40 more genes
    nsv3914334copy number variation1nstd102humanUncertain significance NCBI36 chr5: 60,420,722-60,578,014 , GRCh37.p13 chr5: 60,384,965-60,542,257 , GRCh38.p12 chr5: 61,089,138-61,246,430 NDUFAF2, SMIM15-AS1, 1 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
    nsv3911731copy number variation1nstd102humanPathogenic NCBI36 chr5: 56,279,434-61,056,985 , GRCh38 chr5: 56,947,850-61,725,401 , GRCh37 chr5: 56,243,677-61,021,228 MIR548AE2, RNU6-913P, 52 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
    nsv3888904copy number variation1nstd102humanUncertain significance GRCh37 chr5: 59,753,805-63,274,635 , GRCh38.p12 chr5: 60,457,978-63,978,808 LOC643307, LOC100421561, 42 more genes
    nsv3887618copy number variation1nstd102humanUncertain significance GRCh37 chr5: 59,929,560-61,133,024 , GRCh38.p12 chr5: 60,633,733-61,837,197 LOC105378994, GNL3LP1, 22 more genes
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