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Items: 1 to 20 of 94

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057970inversion1nstd229human GRCh38 chr5: 39,369,727-42,623,585 , GRCh37.p13 chr5: 39,369,829-42,623,687 LINC02996, DAB2, 36 more genes
    nsv6775150copy number variation1nstd229human GRCh38 chr5: 39,513,850-39,940,140 , GRCh37.p13 chr5: 39,513,952-39,940,242 CFAP53P1, INTS6P1, 2 more genes
    nsv6771952copy number variation1nstd229human GRCh38 chr5: 39,525,185-39,528,201 , GRCh37.p13 chr5: 39,525,287-39,528,303 LINC02104
    nsv6769814copy number variation1nstd229human GRCh38 chr5: 39,447,462-42,528,554 , GRCh37.p13 chr5: 39,447,564-42,528,656 RNU7-161P, OXCT1, 35 more genes
    nsv6769429copy number variation1nstd229human GRCh38 chr5: 35,077,787-40,637,192 , GRCh37.p13 chr5: 35,077,889-40,637,294 LINC02110, LOC105374735, 68 more genes
    nsv6769100copy number variation1nstd229human GRCh38 chr5: 39,519,105-39,524,639 , GRCh37.p13 chr5: 39,519,207-39,524,741 LINC02104
    nsv6764301copy number variation1nstd229human GRCh38 chr5: 37,395,324-40,706,253 , GRCh37.p13 chr5: 37,395,426-40,706,355 DAB2, LOC107986414, 39 more genes
    nsv6763460copy number variation1nstd229human GRCh38 chr5: 39,215,959-40,973,214 , GRCh37.p13 chr5: 39,216,061-40,973,316 PRKAA1, PTGER4, 18 more genes
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
    nsv6394858copy number variation1nstd223human GRCh38 chr5: 39,517,581-39,519,192 , GRCh37.p13 chr5: 39,517,683-39,519,294 LINC02104
    nsv6392098copy number variation1nstd223human GRCh38 chr5: 39,525,181-39,528,173 , GRCh37.p13 chr5: 39,525,283-39,528,275 LINC02104
    nsv6388671copy number variation1nstd223human GRCh38 chr5: 39,447,462-42,528,554 , GRCh37.p13 chr5: 39,447,564-42,528,656 SERBP1P6, TCP1P2, 35 more genes
    nsv6384145copy number variation1nstd223human GRCh38 chr5: 39,519,042-39,519,647 , GRCh37.p13 chr5: 39,519,144-39,519,749 LINC02104
    nsv6381382copy number variation1nstd223human GRCh38 chr5: 39,519,102-39,524,638 , GRCh37.p13 chr5: 39,519,204-39,524,740 LINC02104
    nsv6315368copy number variation1nstd102humanPathogenic GRCh37 chr5: 36,053,583-46,389,339 , GRCh38.p12 chr5: 36,053,481-46,389,237 C7, RIMOC1, 128 more genes
    nsv6313864copy number variation1nstd102humanPathogenic GRCh37 chr5: 26,382,110-46,389,339 , GRCh38.p12 chr5: 26,382,001-46,389,237 LOC107986346, RNU6-760P, 227 more genes
    nsv6300383copy number variation1nstd186human GRCh37 chr5: 26,834,087-43,674,516 , GRCh38.p12 chr5: 26,833,978-43,674,414 , TMEM267, 221 more genes
    nsv6136115copy number variation1nstd213human GRCh37 chr5: 39,220,000-39,860,001 , GRCh38.p12 chr5: 39,219,898-39,859,899 C9, DAB2, 4 more genes
    nsv6135664copy number variation1nstd213human GRCh37 chr5: 39,130,000-40,340,001 , GRCh38.p12 chr5: 39,129,898-40,339,899 DAB2, FYB1, 10 more genes
    nsv6135410copy number variation1nstd213human GRCh37 chr5: 38,040,000-43,250,001 , GRCh38.p12 chr5: 38,039,898-43,249,899 FYB1, PTGER4, 78 more genes
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