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Items: 1 to 20 of 282

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097243copy number variation1nstd102humanPathogenic GRCh37 chr4: 178,357,420-178,363,667 , GRCh38.p12 chr4: 177,436,266-177,442,513 AGA-DT, AGA
    nsv7096989copy number variation1nstd102humanPathogenic GRCh37 chr4: 178,351,918-178,357,515 , GRCh38.p12 chr4: 177,430,764-177,436,361 AGA
    nsv7093619copy number variation1nstd228human GRCh37 chr4: 171,508,974-190,957,473 , GRCh38.p12 chr4: 170,587,823-190,036,318 AGA, SLC25A4, 240 more genes
    nsv7056086inversion1nstd229human GRCh38 chr4: 174,912,619-184,252,538 , GRCh37.p13 chr4: 175,833,770-185,173,691 WDR17, LOC105377580, 84 more genes
    nsv7040070inversion1nstd229human GRCh38 chr4: 177,231,111-177,526,060 , GRCh37.p13 chr4: 178,152,265-178,447,214 RNA5SP172, AGA, 4 more genes
    nsv6756227copy number variation1nstd229human GRCh38 chr4: 177,430,325-177,439,157 , GRCh37.p13 chr4: 178,351,479-178,360,311 AGA
    nsv6755547copy number variation1nstd229human GRCh38 chr4: 177,425,365-177,431,144 , GRCh37.p13 chr4: 178,346,519-178,352,298 AGA
    nsv6753732copy number variation1nstd229human GRCh38 chr4: 177,333,192-177,547,079 , GRCh37.p13 chr4: 178,254,346-178,468,233 LOC105377558, AGA, 3 more genes
    nsv6749777copy number variation1nstd229human GRCh38 chr4: 177,441,268-177,445,363 , GRCh37.p13 chr4: 178,362,422-178,366,517 AGA-DT, AGA
    nsv6749610copy number variation1nstd229human GRCh38 chr4: 177,415,562-177,437,907 , GRCh37.p13 chr4: 178,336,716-178,359,061 AGA
    nsv6740598copy number variation1nstd229human GRCh38 chr4: 177,318,312-177,634,231 , GRCh37.p13 chr4: 178,239,466-178,555,385 AGA-DT, NEIL3, 3 more genes
    nsv6740305copy number variation1nstd229human GRCh38 chr4: 177,316,985-177,540,328 , GRCh37.p13 chr4: 178,238,139-178,461,482 RNA5SP172, AGA, 3 more genes
    nsv6739119copy number variation1nstd229human GRCh38 chr4: 177,438,202-177,438,358 , GRCh37.p13 chr4: 178,359,356-178,359,512 AGA
    nsv6634364copy number variation1nstd102humanPathogenic GRCh37 chr4: 167,779,888-190,957,473 , GRCh38.p12 chr4: 166,858,737-190,036,318 LOC101928551, LOC107986330, 279 more genes
    nsv6634351copy number variation1nstd102humanPathogenic GRCh37 chr4: 159,174,483-190,957,473 , GRCh38.p12 chr4: 158,253,331-190,036,318 COPS3P1, LOC339975, 363 more genes
    nsv6629590copy number variation1nstd224human GRCh37 chr4: 178,141,976-179,833,516 , GRCh38.p12 chr4: 177,220,822-178,912,362 AGA-DT, RNA5SP173, 14 more genes
    nsv6570050inversion1nstd223human GRCh38 chr4: 169,780,525-178,315,900 , GRCh37.p13 chr4: 170,701,676-179,237,054 LOC101928409, LOC100131553, 91 more genes
    nsv6383044copy number variation1nstd223human GRCh38 chr4: 177,441,267-177,445,362 , GRCh37.p13 chr4: 178,362,421-178,366,516 AGA-DT, AGA
    nsv6315418copy number variation1nstd102humanUncertain significance GRCh37 chr4: 178,126,365-179,868,269 , GRCh38.p12 chr4: 177,205,211-178,947,115 AGA-DT, LINC01099, 14 more genes
    nsv6315348copy number variation1nstd102humanPathogenic GRCh37 chr4: 174,944,132-190,957,473 , GRCh38.p12 chr4: 174,022,981-190,036,318 SPATA4, ADAM20P2, 203 more genes
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