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Items: 1 to 20 of 102

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7094351copy number variation1nstd102humanUncertain significance GRCh37 chr14: 90,429,459-97,347,545 , GRCh38.p12 chr14: 89,963,115-96,881,208 FBLN5, CYB5AP3, 135 more genes
    nsv7094272copy number variation1nstd102humanUncertain significance GRCh37 chr14: 95,080,779-97,347,545 , GRCh38.p12 chr14: 94,614,442-96,881,208 ADIPOR1P2, LOC105370637, 48 more genes
    nsv7077173inversion1nstd229human GRCh38 chr14: 96,042,489-96,309,879 , GRCh37.p13 chr14: 96,508,826-96,776,216 C14orf132, BDKRB2, 3 more genes
    nsv7059017inversion1nstd229human GRCh38 chr14: 96,226,465-96,562,101 , GRCh37.p13 chr14: 96,692,802-97,028,438 PAPOLA-DT, BDKRB1, 8 more genes
    nsv6977693copy number variation1nstd229human GRCh38 chr14: 96,180,301-96,307,600 , GRCh37.p13 chr14: 96,646,638-96,773,937 BDKRB2, ATG2B, 2 more genes
    nsv6970014copy number variation1nstd229human GRCh38 chr14: 96,262,068-96,262,151 , GRCh37.p13 chr14: 96,728,405-96,728,488 BDKRB1
    nsv6963788copy number variation1nstd229human GRCh38 chr14: 96,159,591-96,327,605 , GRCh37.p13 chr14: 96,625,928-96,793,942 ATG2B, BDKRB2, 2 more genes
    nsv6961855copy number variation1nstd229human GRCh38 chr14: 96,042,501-96,308,000 , GRCh37.p13 chr14: 96,508,838-96,774,337 BDKRB2, ATG2B, 3 more genes
    nsv6960836copy number variation1nstd229human GRCh38 chr14: 96,261,689-96,264,451 , GRCh37.p13 chr14: 96,728,026-96,730,788 BDKRB1
    nsv6637825copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,537,502-107,285,437 , GRCh38.p12 chr14: 84,071,158-106,877,229 CHGA, SNORD114-26, 676 more genes
    nsv6637462copy number variation1nstd102humanLikely pathogenic GRCh37 chr14: 81,593,708-97,059,276 , GRCh38.p12 chr14: 81,127,364-96,592,939 SERPINA3, BDKRB1, 210 more genes
    nsv6500549copy number variation1nstd223human GRCh38 chr14: 96,159,591-96,327,605 , GRCh37.p13 chr14: 96,625,928-96,793,942 ATG2B, BDKRB2, 2 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
    nsv6291768copy number variation1nstd102humanPathogenic GRCh37 chr14: 95,871,795-102,457,523 , GRCh38.p12 chr14: 95,405,458-101,991,186 CCDC85C, MEG3, 206 more genes
    nsv6132796copy number variation1nstd213human GRCh37 chr14: 96,660,000-97,840,001 , GRCh38.p12 chr14: 96,193,663-97,373,664 PAPOLA, ATG2B, 16 more genes
    nsv5505494copy number variation1nstd206human GRCh38 chr14: 96,262,068-96,262,151 , GRCh37.p13 chr14: 96,728,405-96,728,488 BDKRB1
    nsv5498590copy number variation1nstd206human GRCh38 chr14: 80,522,636-106,763,637 , GRCh37.p13 chr14: 80,988,980-106,929,356 , RPS18P2, 713 more genes
    nsv5357579translocation1nstd200human GRCh38 chr14: 96,262,068-96,262,068 , GRCh38 chr14: 96,262,151-96,262,151 , GRCh37.p13 chr14: 96,728,405-96,728,405 , GRCh37.p13 chr14: 96,728,488-96,728,488 BDKRB1
    nsv4675940copy number variation1nstd102humanUncertain significance GRCh37 chr14: 96,509,822-96,832,238 , GRCh38.p12 chr14: 96,043,485-96,365,901 CKS1BP1, BDKRB1, 4 more genes
    nsv4675107copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,783,523-96,907,490 , GRCh38.p12 chr14: 84,317,179-96,441,153 SHLD2P2, RPL15P2, 175 more genes
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