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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4948849copy number variation1nstd200human GRCh38 chr5: 66,152,539-66,983,998 , GRCh37.p13 chr5: 65,448,367-66,279,826 SREK1, MAST4, 6 more genes
    nsv4937627copy number variation1nstd200human GRCh38 chr5: 66,202,453-66,228,255 , GRCh37.p13 chr5: 65,498,281-65,524,083 LINC02065
    nsv4803307copy number variation1nstd200human GRCh37 chr5: 65,498,281-65,524,083 , GRCh38.p12 chr5: 66,202,453-66,228,255 LINC02065
    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
    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
    nsv4124835copy number variation1nstd166human GRCh37.p13 chr5: 65,448,367-66,279,770 , GRCh38.p12 chr5: 66,152,539-66,983,942 SREK1, PPIAP78, 6 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
    nsv3921568copy number variation1nstd102humanPathogenic GRCh37 chr5: 64,228,590-68,791,331 , NCBI36 chr5: 64,264,346-68,827,087 , GRCh38 chr5: 64,932,763-69,495,504 LOC100419549, MAST4-AS1, 67 more genes
    nsv3920547copy number variation1nstd102humanUncertain significance GRCh38 chr5: 65,976,124-71,317,474 , NCBI36 chr5: 65,307,708-70,649,057 , GRCh37 chr5: 65,271,952-70,613,301 SMN1, NAIP, 97 more genes
    nsv3920421copy number variation1nstd102humanLikely pathogenic NCBI36 chr5: 62,538,695-70,622,774 , GRCh37 chr5: 62,502,939-70,587,018 , GRCh38 chr5: 63,207,112-71,291,191 TRIM23, CCNB1, 124 more genes
    nsv3916989copy number variation1nstd102humanUncertain significance NCBI36 chr5: 64,543,311-66,078,345 , GRCh37 chr5: 64,507,555-66,042,589 , GRCh38 chr5: 65,211,728-66,746,761 LINC02229, TRIM23, 20 more genes
    nsv3916577copy number variation1nstd102humanLikely pathogenic NCBI36 chr5: 64,745,346-65,762,306 , GRCh37 chr5: 64,709,590-65,726,550 , GRCh38 chr5: 65,413,763-66,430,722 TRIM23, ADAMTS6, 15 more genes
    nsv3912692copy number variation1nstd102humanUncertain significance GRCh38 chr5: 66,201,296-68,094,987 , GRCh37 chr5: 65,497,124-67,390,815 , NCBI36 chr5: 65,532,880-67,426,571 LOC105379004, RPL21P55, 15 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
    nsv3883692copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 58,966,132-68,847,066 , GRCh38.p12 chr5: 59,670,306-69,551,239 TRIM23, CCNB1, 125 more genes
    nsv3875235copy number variation2nstd102humanPathogenic GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788 SPEF2, NDST1, 2490 more genes
    nsv3875076copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 65,315,606-68,755,816 , GRCh38.p12 chr5: 66,019,778-69,459,989 CCNB1, CDK7, 47 more genes
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