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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148206copy number variation1nstd102humanPathogenic GRCh38 chr1: 197,435,257-197,441,674 , GRCh37.p13 chr1: 197,404,387-197,410,804 CRB1
    nsv7099255copy number variation1nstd231human GRCh38.p12 chr1: 192,358,641-201,911,882 , GRCh37 chr1: 192,327,771-201,881,010 CACNA1S, CSRP1, 120 more genes
    nsv7095954copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 197,325,941-197,326,163 , GRCh38.p12 chr1: 197,356,811-197,357,033 CRB1
    nsv7095775copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,407,657-197,411,442 , GRCh38.p12 chr1: 197,438,527-197,442,312 CRB1
    nsv7095774copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,390,110-197,391,106 , GRCh38.p12 chr1: 197,420,980-197,421,976 CRB1
    nsv7095773copy number variation1nstd102humanLikely pathogenic GRCh37 chr1: 197,313,391-197,411,442 , GRCh38.p12 chr1: 197,344,261-197,442,312 CRB1, MRPS21P3
    nsv7095772copy number variation1nstd102humanUncertain significance GRCh37 chr1: 197,297,532-197,447,009 , GRCh38.p12 chr1: 197,328,402-197,477,879 MRPS21P3, CRB1
    nsv7095771copy number variation1nstd102humanUncertain significance GRCh37 chr1: 197,297,532-197,326,163 , GRCh38.p12 chr1: 197,328,402-197,357,033 CRB1
    nsv7095500copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,407,736-197,423,021 , GRCh38.p12 chr1: 197,438,606-197,453,891 CRB1
    nsv7095499copy number variation1nstd102humanUncertain significance GRCh37 chr1: 197,237,543-197,237,632 , GRCh38.p12 chr1: 197,268,413-197,268,502 CRB1
    nsv7095498copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,237,324-197,447,595 , GRCh38.p12 chr1: 197,268,194-197,478,465 MRPS21P3, CRB1
    nsv7093373copy number variation1nstd102humanUncertain significance GRCh37 chr1: 196,670,448-197,898,389 , GRCh38.p12 chr1: 196,701,318-197,929,259 LHX9, ASPM, 19 more genes
    nsv7093328copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,396,981-197,397,052 , GRCh38 chr1: 197,427,851-197,427,922 CRB1
    nsv7047291inversion1nstd229human GRCh38 chr1: 197,300,186-197,300,624 , GRCh37.p13 chr1: 197,269,316-197,269,754 CRB1
    nsv7046755inversion1nstd229human GRCh38 chr1: 197,153,978-198,848,199 , GRCh37.p13 chr1: 197,123,108-198,817,328 FAM204BP, RPL24P5, 15 more genes
    nsv7044345inversion1nstd229human GRCh38 chr1: 196,256,799-197,729,314 , GRCh37.p13 chr1: 196,225,929-197,698,444 EEF1A1P32, MIR4735, 17 more genes
    nsv7041725inversion1nstd229human GRCh38 chr1: 197,300,397-197,300,580 , GRCh37.p13 chr1: 197,269,527-197,269,710 CRB1
    nsv6677574copy number variation1nstd229human GRCh38 chr1: 197,436,047-197,462,126 , GRCh37.p13 chr1: 197,405,177-197,431,256 CRB1
    nsv6676680copy number variation1nstd229human GRCh38 chr1: 197,201,301-197,208,500 , GRCh37.p13 chr1: 197,170,431-197,177,630 ZBTB41, CRB1
    nsv6676586copy number variation1nstd229human GRCh38 chr1: 197,380,060-197,393,015 , GRCh37.p13 chr1: 197,349,190-197,362,145 CRB1
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