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Items: 1 to 20 of 213

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7147448copy number variation1nstd232human GRCh37.p13 chr3: 186,508,043-186,508,112 , GRCh38.p12 chr3: 186,790,254-186,790,323 EIF4A2, RFC4
    nsv7146492insertion1nstd232human GRCh37.p13 chr3: 186,510,399-186,510,399 , GRCh38.p12 chr3: 186,792,610-186,792,610 RFC4
    nsv7144618insertion1nstd232human GRCh37.p13 chr3: 186,509,643-186,509,643 , GRCh38.p12 chr3: 186,791,854-186,791,854 RFC4
    nsv7141958copy number variation1nstd232human GRCh37.p13 chr3: 186,507,852-186,507,928 , GRCh38.p12 chr3: 186,790,063-186,790,139 EIF4A2, RFC4
    nsv7096951copy number variation2nstd102humanUncertain significance GRCh37 chr3: 186,256,485-187,009,420 , GRCh38.p12 chr3: 186,538,696-187,291,632 AHSG, ST6GAL1, 32 more genes
    nsv7052431inversion1nstd229human GRCh38 chr3: 186,797,746-186,802,390 , GRCh37.p13 chr3: 186,515,535-186,520,179 RFC4
    nsv7040429inversion1nstd229human GRCh38 chr3: 184,379,670-192,292,047 , GRCh37.p13 chr3: 184,097,458-192,009,836 LOC107986163, RPL34P10, 123 more genes
    nsv6736600copy number variation1nstd229human GRCh38 chr3: 186,789,602-186,792,762 , GRCh37.p13 chr3: 186,507,391-186,510,551 EIF4A2, RFC4
    nsv6736371copy number variation1nstd229human GRCh38 chr3: 186,789,763-187,310,322 , GRCh37.p13 chr3: 186,507,552-187,028,110 RPS20P14, LOC101929106, 13 more genes
    nsv6732468copy number variation1nstd229human GRCh38 chr3: 186,791,435-187,004,241 , GRCh37.p13 chr3: 186,509,224-186,722,029 ADIPOQ-AS1, LINC02043, 5 more genes
    nsv6731232copy number variation1nstd229human GRCh38 chr3: 186,406,559-187,159,867 , GRCh37.p13 chr3: 186,124,348-186,877,655 PET100P1, SNORA81, 30 more genes
    nsv6722471copy number variation1nstd229human GRCh38 chr3: 186,789,774-186,896,030 , GRCh37.p13 chr3: 186,507,563-186,613,819 LINC02043, ADIPOQ-AS1, 3 more genes
    nsv6720864copy number variation1nstd229human GRCh38 chr3: 186,786,474-186,794,820 , GRCh37.p13 chr3: 186,504,263-186,512,609 SNORA63, MIR1248, 5 more genes
    nsv6718098copy number variation1nstd229human GRCh38 chr3: 186,784,216-186,959,926 , GRCh37.p13 chr3: 186,502,005-186,677,714 SNORA63B, LINC02043, 12 more genes
    nsv6636645copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 184,170,962-188,047,867 , GRCh38.p12 chr3: 184,453,174-188,330,079 AHSG, BCL6, 80 more genes
    nsv6634371copy number variation1nstd102humanLikely pathogenic GRCh37 chr3: 171,549,421-198,022,430 , GRCh38.p12 chr3: 171,831,631-198,235,559 ACTL6A, AHSG, 466 more genes
    nsv6628929copy number variation1nstd224human GRCh37 chr3: 186,328,121-186,710,637 , GRCh38.p12 chr3: 186,610,332-186,992,849 AHSG, EIF4A2, 21 more genes
    nsv6565296inversion1nstd223human GRCh38 chr3: 186,799,730-186,800,108 , GRCh37.p13 chr3: 186,517,519-186,517,897 RFC4
    nsv6368922copy number variation1nstd223human GRCh38 chr3: 186,786,474-186,794,823 , GRCh37.p13 chr3: 186,504,263-186,512,612 SNORA4, SNORA81, 5 more genes
    nsv6366089copy number variation1nstd223human GRCh38 chr3: 186,790,035-186,919,129 , GRCh37.p13 chr3: 186,507,824-186,636,918 ADIPOQ, RPS20P14, 4 more genes
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