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Items: 1 to 20 of 117

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055630inversion1nstd229human GRCh38 chr5: 66,647,773-71,648,116 , GRCh37.p13 chr5: 65,943,601-70,943,943 OCLNP1, CDK7, 96 more genes
    nsv6776721copy number variation1nstd229human GRCh38 chr5: 67,193,933-67,233,603 , GRCh37.p13 chr5: 66,489,761-66,529,431 CD180
    nsv6763618copy number variation1nstd229human GRCh38 chr5: 66,450,908-74,585,645 , GRCh37.p13 chr5: 65,746,736-73,881,470 LOC107986372, LOC105379027, 146 more genes
    nsv6636291copy number variation1nstd102humanUncertain significance GRCh37 chr5: 66,424,994-66,710,524 , GRCh38.p12 chr5: 67,129,166-67,414,696 CD180, MAST4
    nsv6398598copy number variation1nstd223human GRCh38 chr5: 67,129,344-67,410,879 , GRCh37.p13 chr5: 66,425,172-66,706,707 MAST4, CD180
    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
    nsv6291416copy number variation1nstd102humanUncertain significance GRCh37 chr5: 65,936,855-66,783,546 , GRCh38.p12 chr5: 66,641,027-67,487,718 MAST4, LOC101928819, 2 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
    nsv4937656copy number variation1nstd200human GRCh38 chr5: 67,189,354-67,191,266 , GRCh37.p13 chr5: 66,485,182-66,487,094 CD180
    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
    nsv4484323mobile element insertion1nstd166human GRCh37.p13 chr5: 66,478,904-66,478,904 , GRCh38.p12 chr5: 67,183,076-67,183,076 CD180
    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
    nsv4129826copy number variation1nstd166human GRCh37.p13 chr5: 66,489,761-66,529,431 , GRCh38.p12 chr5: 67,193,933-67,233,603 CD180
    nsv4121544copy number variation1nstd166human GRCh37.p13 chr5: 66,477,305-66,477,992 , GRCh38.p12 chr5: 67,181,477-67,182,164 CD180
    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
    nsv4113646copy number variation1nstd166human GRCh37.p13 chr5: 66,482,627-66,482,867 , GRCh38.p12 chr5: 67,186,799-67,187,039 CD180
    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
    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
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