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Items: 1 to 20 of 138

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6977937copy number variation1nstd229human GRCh38 chr14: 75,538,079-75,539,753 , GRCh37.p13 chr14: 76,004,422-76,006,096 BATF
    nsv6974940copy number variation1nstd229human GRCh38 chr14: 75,523,370-76,313,567 , GRCh37.p13 chr14: 75,989,713-76,779,910 LOC107984653, LOC100506576, 13 more genes
    nsv6970692copy number variation1nstd229human GRCh38 chr14: 75,543,813-75,635,380 , GRCh37.p13 chr14: 76,010,156-76,101,723 FLVCR2, RNA5SP387, 4 more genes
    nsv6966940copy number variation1nstd229human GRCh38 chr14: 75,469,256-75,636,208 , GRCh37.p13 chr14: 75,935,959-76,102,551 BATF, RPS24P2, 6 more genes
    nsv6964648copy number variation1nstd229human GRCh38 chr14: 75,255,601-75,729,300 , GRCh37.p13 chr14: 75,722,304-76,195,643 LOC107984653, ERG28, 12 more genes
    nsv6961278copy number variation1nstd229human GRCh38 chr14: 75,528,583-75,531,152 , GRCh37.p13 chr14: 75,994,926-75,997,495 BATF
    nsv6961105copy number variation1nstd229human GRCh38 chr14: 75,539,921-75,540,300 , GRCh37.p13 chr14: 76,006,264-76,006,643 BATF
    nsv6495564copy number variation1nstd223human GRCh38 chr14: 75,538,079-75,539,753 , GRCh37.p13 chr14: 76,004,422-76,006,096 BATF
    nsv6488919copy number variation1nstd223human GRCh38 chr14: 75,469,256-75,636,209 , GRCh37.p13 chr14: 75,935,959-76,102,552 FLVCR2-AS1, LOC107984653, 6 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 PAPOLA-DT, LOC105378180, 1338 more genes
    nsv6241534mobile element insertion1nstd215human GRCh38 chr14: 75,539,451-75,539,451 , GRCh37.p13 chr14: 76,005,794-76,005,794 BATF
    nsv5703065mobile element insertion2nstd211human GRCh38 chr14: 75,539,451-75,539,451 , GRCh37.p13 chr14: 76,005,794-76,005,794 BATF
    nsv5510249copy number variation1nstd206human GRCh38 chr14: 75,523,919-75,534,748 , GRCh37.p13 chr14: 75,990,262-76,001,091 BATF
    nsv5340434translocation1nstd200human GRCh37 chr14: 75,999,731-75,999,731 , GRCh37 chr14: 75,999,643-75,999,643 , GRCh38.p12 chr14: 75,533,300-75,533,300 , GRCh38.p12 chr14: 75,533,388-75,533,388 BATF
    nsv5032025inversion1nstd200human GRCh38 chr14: 53,190,097-88,878,877 , GRCh37.p13 chr14: 53,656,815-89,345,221 , IFT43, 578 more genes
    nsv5000107copy number variation1nstd200human GRCh38 chr14: 75,536,424-75,537,004 , GRCh37.p13 chr14: 76,002,767-76,003,347 BATF
    nsv5000106copy number variation1nstd200human GRCh38 chr14: 75,533,300-75,533,388 , GRCh37.p13 chr14: 75,999,643-75,999,731 BATF
    nsv5000105copy number variation1nstd200human GRCh38 chr14: 75,525,481-75,529,418 , GRCh37.p13 chr14: 75,991,824-75,995,761 BATF
    nsv4838782copy number variation1nstd200human GRCh37 chr14: 76,002,767-76,003,347 , GRCh38.p12 chr14: 75,536,424-75,537,004 BATF
    nsv4680388copy number variation1nstd189human GRCh37.p13 chr14: 75,863,813-76,042,536 , GRCh38.p12 chr14: 75,397,110-75,576,193 , BATF, 5 more genes
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