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Items: 1 to 20 of 267

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055071inversion1nstd229human GRCh38 chr1: 43,970,005-47,371,780 , GRCh37.p13 chr1: 44,435,677-47,837,452 SNORD38A, PPIAP36, 121 more genes
    nsv7047736inversion1nstd229human GRCh38 chr1: 46,778,787-47,065,120 , GRCh37.p13 chr1: 47,244,459-47,530,792 CYP4X1, CYP4A11, 8 more genes
    nsv7046201inversion1nstd229human GRCh38 chr1: 45,964,231-47,257,863 , GRCh37.p13 chr1: 46,429,903-47,723,535 TUBAP9, MKNK1-AS1, 45 more genes
    nsv7043792inversion1nstd229human GRCh38 chr1: 46,858,248-46,906,328 , GRCh37.p13 chr1: 47,323,920-47,372,000 TUBAP8, CYP4Z2P
    nsv7039549inversion1nstd229human GRCh38 chr1: 46,877,665-46,974,291 , GRCh37.p13 chr1: 47,343,337-47,439,963 CYP4A11, CYP4X1, 3 more genes
    nsv7038609inversion1nstd229human GRCh38 chr1: 46,854,623-47,111,224 , GRCh37.p13 chr1: 47,320,295-47,576,896 CYP4A44P, CYP4Z1, 8 more genes
    nsv6650776copy number variation1nstd229human GRCh38 chr1: 46,875,901-46,882,000 , GRCh37.p13 chr1: 47,341,573-47,347,672 CYP4Z2P
    nsv6650701copy number variation1nstd229human GRCh38 chr1: 46,875,501-46,881,400 , GRCh37.p13 chr1: 47,341,173-47,347,072 CYP4Z2P
    nsv6650700copy number variation1nstd229human GRCh38 chr1: 46,851,047-46,968,873 , GRCh37.p13 chr1: 47,316,719-47,434,545 CYP4A11, CYP4Z2P, 3 more genes
    nsv6650561copy number variation1nstd229human GRCh38 chr1: 46,745,716-46,854,830 , GRCh37.p13 chr1: 47,211,388-47,320,502 LOC105378699, CYP4Z2P, 1 more genes
    nsv6626029copy number variation1nstd224human GRCh37 chr1: 47,349,901-47,614,425 , GRCh38.p12 chr1: 46,884,229-47,148,753 CYP4Z1, TUBAP9, 9 more genes
    nsv6626028copy number variation1nstd224human GRCh37 chr1: 47,259,138-47,392,054 , GRCh38.p12 chr1: 46,793,466-46,926,382 CYP4B1, CYP4Z2P, 1 more genes
    nsv6330877copy number variation1nstd223human GRCh38 chr1: 46,745,716-46,854,830 , GRCh37.p13 chr1: 47,211,388-47,320,502 CYP4Z2P, CYP4B1, 1 more genes
    nsv6319986copy number variation1nstd223human GRCh38 chr1: 46,867,724-46,870,254 , GRCh37.p13 chr1: 47,333,396-47,335,926 CYP4Z2P
    nsv6313688copy number variation1nstd102humanPathogenic GRCh37 chr1: 33,285,582-47,891,811 , GRCh38.p12 chr1: 32,819,981-47,426,139 LOC107984940, PPIAP36, 407 more genes
    nsv6298522copy number variation1nstd186human GRCh37 chr1: 47,342,507-47,348,507 , GRCh38.p12 chr1: 46,876,835-46,882,835 CYP4Z2P
    nsv6147179sequence alteration1nstd206human GRCh38 chr1: 46,855,668-47,110,483 , GRCh37.p13 chr1: 47,321,340-47,576,155 CYP4Z1, CYP4A43P, 8 more genes
    nsv6138733copy number variation1nstd206human GRCh38 chr1: 46,885,835-46,935,835 , GRCh37.p13 chr1: 47,351,507-47,401,507 CYP4Z2P, CYP4A11, 1 more genes
    nsv6133997copy number variation1nstd213human GRCh37 chr1: 46,960,000-47,650,001 , GRCh38.p12 chr1: 46,494,328-47,184,329 CYP4A11, CYP4B1, 28 more genes
    nsv5984589copy number variation1nstd212human GRCh38 chr1: 46,882,538-46,898,450 , GRCh37.p13 chr1: 47,348,210-47,364,122 TUBAP8, CYP4Z2P
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