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Items: 1 to 20 of 106

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7040565inversion1nstd229human GRCh38 chr5: 65,352,482-65,851,740 , GRCh37.p13 chr5: 64,648,309-65,147,568 LOC100419549, RPS2P23, 9 more genes
    nsv6777129copy number variation1nstd229human GRCh38 chr5: 65,517,434-66,063,747 , GRCh37.p13 chr5: 64,813,261-65,359,575 TRIM23, RNU6-540P, 9 more genes
    nsv6765694copy number variation1nstd229human GRCh38 chr5: 65,469,125-65,655,579 , GRCh37.p13 chr5: 64,764,952-64,951,406 PPWD1, SHLD3, 5 more genes
    nsv6765339copy number variation1nstd229human GRCh38 chr5: 65,595,125-65,604,197 , GRCh37.p13 chr5: 64,890,952-64,900,024 RNU6-540P, TRIM23
    nsv6765273copy number variation1nstd229human GRCh38 chr5: 65,460,432-65,973,179 , GRCh37.p13 chr5: 64,756,259-65,269,007 NLN, RNU6-540P, 10 more genes
    nsv6313676copy number variation1nstd102humanPathogenic GRCh37 chr5: 64,049,692-70,306,646 , GRCh38.p12 chr5: 64,753,865-71,010,819 BCL9P1, CWC27, 105 more genes
    nsv6312114copy number variation1nstd102humanPathogenic GRCh37 chr5: 63,256,278-65,374,358 , GRCh38.p12 chr5: 63,960,451-66,078,530 RNF180, RPEP1, 23 more genes
    nsv6136128copy number variation1nstd213human GRCh37 chr5: 62,820,000-66,080,001 , GRCh38.p12 chr5: 63,524,173-66,784,173 TRIM23, HTR1A, 33 more genes
    nsv6135416copy number variation1nstd213human GRCh37 chr5: 50,510,000-68,870,001 , GRCh38.p12 chr5: 51,214,166-69,574,174 , TRIM23, 243 more genes
    nsv6135192copy number variation1nstd213human GRCh37 chr5: 63,780,000-66,290,001 , GRCh38.p12 chr5: 64,484,173-66,994,173 TRIM23, CWC27, 29 more genes
    nsv4937610copy number variation1nstd200human GRCh38 chr5: 65,565,681-65,627,967 , GRCh37.p13 chr5: 64,861,508-64,923,794 RNU6-540P, SHLD3, 3 more genes
    nsv4675585copy number variation1nstd102humanUncertain significance GRCh37 chr5: 64,775,928-64,994,289 , GRCh38.p12 chr5: 65,480,101-65,698,462 ADAMTS6, PPWD1, 6 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
    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
    nsv4388209copy number variation1nstd173human GRCh37 chr5: 64,827,304-65,023,563 , GRCh38.p12 chr5: 65,531,477-65,727,736 TRIM23, PPWD1, 6 more genes
    nsv4378244copy number variation1nstd173human GRCh37 chr5: 64,837,193-65,023,563 , GRCh38.p12 chr5: 65,541,366-65,727,736 TRIM23, PPWD1, 6 more genes
    nsv4125346copy number variation1nstd166human GRCh37.p13 chr5: 64,756,246-65,269,007 , GRCh38.p12 chr5: 65,460,419-65,973,179 CENPK, PPWD1, 10 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
    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
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