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Items: 1 to 20 of 229

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099297copy number variation1nstd231human GRCh38.p12 chr1: 58,444,770-67,143,664 , GRCh37 chr1: 58,910,442-67,609,347 AK4, CYP2J2, 125 more genes
    nsv7099210copy number variation1nstd231human GRCh38.p12 chr1: 66,256,800-84,953,993 , GRCh37 chr1: 66,722,483-85,419,676 ACADM, COX6A1P1, 211 more genes
    nsv7095627copy number variation1nstd102humanPathogenic GRCh37 chr1: 61,548,464-67,861,772 , GRCh38.p12 chr1: 61,082,792-67,396,089 ALG6, MIR3116-2, 94 more genes
    nsv7095538copy number variation1nstd102humanPathogenic GRCh37 chr1: 65,299,551-67,861,772 , GRCh38.p12 chr1: 64,833,868-67,396,089 MRPS21P1, MIER1, 36 more genes
    nsv7055498inversion1nstd229human GRCh38 chr1: 66,514,766-73,182,042 , GRCh37.p13 chr1: 66,980,449-73,647,725 LINC02796, LOC105378789, 80 more genes
    nsv7054976inversion1nstd229human GRCh38 chr1: 66,778,824-69,400,485 , GRCh37.p13 chr1: 67,244,507-69,866,168 ELOCP18, MIR1262, 40 more genes
    nsv6653703copy number variation1nstd229human GRCh38 chr1: 67,124,252-67,128,591 , GRCh37.p13 chr1: 67,589,935-67,594,274 C1orf141
    nsv6653701copy number variation1nstd229human GRCh38 chr1: 67,091,301-67,109,100 , GRCh37.p13 chr1: 67,556,984-67,574,783 C1orf141
    nsv6653388copy number variation1nstd229human GRCh38 chr1: 67,106,225-67,110,773 , GRCh37.p13 chr1: 67,571,908-67,576,456 C1orf141
    nsv6653387copy number variation1nstd229human GRCh38 chr1: 67,099,412-67,099,440 , GRCh37.p13 chr1: 67,565,095-67,565,123 C1orf141
    nsv6653386copy number variation1nstd229human GRCh38 chr1: 67,097,101-67,136,400 , GRCh37.p13 chr1: 67,562,784-67,602,083 C1orf141
    nsv6653250copy number variation1nstd229human GRCh38 chr1: 67,113,875-67,117,657 , GRCh37.p13 chr1: 67,579,558-67,583,340 C1orf141
    nsv6653249copy number variation1nstd229human GRCh38 chr1: 67,093,346-67,109,103 , GRCh37.p13 chr1: 67,559,029-67,574,786 C1orf141
    nsv6626276copy number variation1nstd224human GRCh37 chr1: 67,580,350-67,633,812 , GRCh38.p12 chr1: 67,114,667-67,168,129 IL23R, C1orf141
    nsv6554169inversion1nstd223human GRCh38 chr1: 67,123,981-67,124,837 , GRCh37.p13 chr1: 67,589,664-67,590,520 C1orf141
    nsv6548301inversion1nstd223human GRCh38 chr1: 67,122,093-67,123,199 , GRCh37.p13 chr1: 67,587,776-67,588,882 C1orf141
    nsv6543803inversion1nstd223human GRCh38 chr1: 67,127,651-67,128,424 , GRCh37.p13 chr1: 67,593,334-67,594,107 C1orf141
    nsv6542615inversion1nstd223human GRCh38 chr1: 67,131,561-67,132,296 , GRCh37.p13 chr1: 67,597,244-67,597,979 C1orf141
    nsv6542115inversion1nstd223human GRCh38 chr1: 61,925,268-71,371,290 , GRCh37.p13 chr1: 62,390,940-71,836,973 PATJ, GNG12-AS1, 142 more genes
    nsv6334507copy number variation1nstd223human GRCh38 chr1: 67,113,799-67,117,154 , GRCh37.p13 chr1: 67,579,482-67,582,837 C1orf141
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