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    Number of Variants: 13

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6291443copy number variation1nstd102humanUncertain significance GRCh37 chr5: 63,728,460-63,853,032 , GRCh38.p12 chr5: 64,432,633-64,557,205 RGS7BP, RN7SL169P
    nsv3889848copy number variation1nstd102humanPathogenic GRCh37 chr5: 17,628,741-176,575,720 , GRCh38.p12 chr5: 17,628,632-177,148,719 RGS7BP, MEGF10, 2080 more genes
    nsv6312114copy number variation1nstd102humanPathogenic GRCh37 chr5: 63,256,278-65,374,358 , GRCh38.p12 chr5: 63,960,451-66,078,530 RGS7BP, RNF180, 23 more genes
    nsv3886374copy number variation1nstd102humanPathogenic GRCh37 chr5: 13,648-180,905,029 , GRCh38.p12 chr5: 13,648-181,478,028 RGS7BP, LOC105374618, 2499 more genes
    nsv3871533copy number variation1nstd102humanPathogenic GRCh37 chr5: 25,328-180,693,344 , GRCh38.p12 chr5: 25,329-181,266,343 RGS7BP, PCDHGC5, 2492 more genes
    nsv3875235copy number variation2nstd102humanPathogenic GRCh37 chr5: 113,577-180,719,789 , GRCh38.p12 chr5: 113,462-181,292,788 RGS7BP, SPEF2, 2490 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 RGS7BP, LINC02241, 878 more genes
    nsv4578696copy number variation1nstd102humanLikely pathogenic GRCh38 chr5: 58,780,641-73,523,380 , GRCh37.p13 chr5: 58,076,468-72,819,205 RGS7BP, TRIM23, 215 more genes
    nsv3883692copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 58,966,132-68,847,066 , GRCh38.p12 chr5: 59,670,306-69,551,239 RGS7BP, TRIM23, 125 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 RGS7BP, TRIM23, 124 more genes
    nsv4436202copy number variation1nstd102humanUncertain significance GRCh37 chr5: 14,685,137-149,511,942 , GRCh38.p12 chr5: 14,685,028-150,132,379 RGS7BP, RNU1-150P, 1757 more genes
    nsv4729221copy number variation1nstd102humanUncertain significance GRCh37 chr5: 63,827,760-64,499,916 , GRCh38.p12 chr5: 64,531,933-65,204,089 RGS7BP, SREK1IP1, 7 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 RGS7BP, LOC105378993, 2492 more genes
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