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Items: 1 to 20 of 302

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6775159copy number variation1nstd229human GRCh38 chr5: 72,201,221-72,201,250 , GRCh37.p13 chr5: 71,497,048-71,497,077 MAP1B
    nsv6774661copy number variation1nstd229human GRCh38 chr5: 72,142,359-72,143,813 , GRCh37.p13 chr5: 71,438,186-71,439,640 MAP1B
    nsv6773916copy number variation1nstd229human GRCh38 chr5: 72,146,395-72,152,300 , GRCh37.p13 chr5: 71,442,222-71,448,127 MAP1B
    nsv6770915copy number variation1nstd229human GRCh38 chr5: 72,123,501-72,129,700 , GRCh37.p13 chr5: 71,419,328-71,425,527 MAP1B
    nsv6768848copy number variation1nstd229human GRCh38 chr5: 72,160,576-72,160,776 , GRCh37.p13 chr5: 71,456,403-71,456,603 MAP1B
    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
    nsv6759145copy number variation1nstd229human GRCh38 chr5: 72,173,152-72,176,296 , GRCh37.p13 chr5: 71,468,979-71,472,123 MAP1B
    nsv6758714copy number variation1nstd229human GRCh38 chr5: 72,193,081-72,193,295 , GRCh37.p13 chr5: 71,488,908-71,489,122 MAP1B
    nsv6758175copy number variation1nstd229human GRCh38 chr5: 72,153,243-72,157,125 , GRCh37.p13 chr5: 71,449,070-71,452,952 MAP1B
    nsv6562140inversion1nstd223human GRCh38 chr5: 72,109,273-72,109,397 , GRCh37.p13 chr5: 71,405,100-71,405,224 MAP1B, LOC105379028
    nsv6406793copy number variation1nstd223human GRCh38 chr5: 72,142,702-72,143,452 , GRCh37.p13 chr5: 71,438,529-71,439,279 MAP1B
    nsv6397554copy number variation1nstd223human GRCh38 chr5: 72,141,932-72,142,500 , GRCh37.p13 chr5: 71,437,759-71,438,327 MAP1B
    nsv6260487mobile element insertion1nstd215human GRCh38 chr5: 72,125,897-72,125,897 , GRCh37.p13 chr5: 71,421,724-71,421,724 MAP1B
    nsv6260486mobile element insertion1nstd215human GRCh38 chr5: 72,117,136-72,117,136 , GRCh37.p13 chr5: 71,412,963-71,412,963 MAP1B
    nsv6136131copy number variation1nstd213human GRCh37 chr5: 70,130,000-73,760,001 , GRCh38.p12 chr5: 70,834,173-74,464,176 , BTF3, 69 more genes
    nsv6135436copy number variation1nstd213human GRCh37 chr5: 70,260,000-91,630,001 , GRCh38.p12 chr5: 70,964,173-92,334,184 , ARSB, 300 more genes
    nsv6135435copy number variation1nstd213human GRCh37 chr5: 69,990,000-73,820,001 , GRCh38.p12 chr5: 70,694,173-74,524,176 , BTF3, 71 more genes
    nsv6135198copy number variation1nstd213human GRCh37 chr5: 70,130,000-76,140,001 , GRCh38.p12 chr5: 70,834,173-76,844,176 , BTF3, 117 more genes
    nsv6078472insertion1nstd212human GRCh38 chr5: 72,117,132-72,117,132 , GRCh37.p13 chr5: 71,412,959-71,412,959 MAP1B
    nsv5952919insertion1nstd209human GRCh38 chr5: 72,117,121-72,117,121 , GRCh37.p13 chr5: 71,412,948-71,412,948 MAP1B
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