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Items: 1 to 20 of 119

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7054358inversion1nstd229human GRCh38 chr5: 98,762,863-98,778,887 , GRCh37.p13 chr5: 98,098,567-98,114,591 RGMB, RGMB-AS1
    nsv7053539inversion1nstd229human GRCh38 chr5: 98,445,677-99,930,756 , GRCh37.p13 chr5: 97,781,381-99,266,460 RNU6-402P, LINC02113, 13 more genes
    nsv7051342inversion1nstd229human GRCh38 chr5: 97,407,672-100,329,439 , GRCh37.p13 chr5: 96,743,376-99,665,143 LOC100420130, CHD1, 40 more genes
    nsv7044198inversion1nstd229human GRCh38 chr5: 93,856,097-99,790,151 , GRCh37.p13 chr5: 93,191,803-99,125,855 FAM81B, LOC107986365, 78 more genes
    nsv6772593copy number variation1nstd229human GRCh38 chr5: 97,940,994-99,097,859 , GRCh37.p13 chr5: 97,276,698-98,433,563 RGMB, LOC100420130, 18 more genes
    nsv6771444copy number variation1nstd229human GRCh38 chr5: 97,916,439-98,775,307 , GRCh37.p13 chr5: 97,252,143-98,111,011 RGMB, LOC100420130, 11 more genes
    nsv6770091copy number variation1nstd229human GRCh38 chr5: 97,800,415-101,500,171 , GRCh37.p13 chr5: 97,136,119-100,835,875 CHD1, LOC100420130, 45 more genes
    nsv6760423copy number variation1nstd229human GRCh38 chr5: 98,748,828-98,844,919 , GRCh37.p13 chr5: 98,084,532-98,180,623 CSNK1A1P3, LOC105379099, 2 more genes
    nsv6637053copy number variation1nstd102humanUncertain significance GRCh37 chr5: 97,280,913-98,343,588 , GRCh38.p12 chr5: 97,945,209-99,007,884 LOC402221, RGMB-AS1, 17 more genes
    nsv6313580copy number variation1nstd102humanPathogenic GRCh37 chr5: 93,650,000-114,969,108 , GRCh38.p12 chr5: 94,314,295-115,633,411 FER, HMGN1P15, 222 more genes
    nsv6135689copy number variation1nstd213human GRCh37 chr5: 96,670,000-113,570,001 , GRCh38.p12 chr5: 97,334,296-114,234,304 APC, CAMK4, 154 more genes
    nsv6135445copy number variation1nstd213human GRCh37 chr5: 98,030,000-98,350,001 , GRCh38.p12 chr5: 98,694,296-99,014,297 CHD1, RGMB, 7 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv5036421inversion1nstd200human GRCh38 chr5: 85,193,812-162,906,830 , GRCh37.p13 chr5: 84,489,630-162,333,836 , PRR16, 1116 more genes
    nsv5033775inversion1nstd200human GRCh38 chr5: 76,373,686-102,541,075 , GRCh37.p13 chr5: 75,669,511-101,876,779 , F2RL1, 331 more genes
    nsv4947215copy number variation1nstd200human GRCh38 chr5: 93,957,557-155,223,076 , GRCh37.p13 chr5: 93,293,262-154,602,636 , TGFBI, 937 more genes
    nsv4885569inversion1nstd200human GRCh37 chr5: 84,489,636-162,333,841 , GRCh38.p12 chr5: 85,193,818-162,906,835 , UBE2B, 1116 more genes
    nsv4872282inversion1nstd200human GRCh37 chr5: 98,106,197-132,803,784 , GRCh38.p12 chr5: 98,770,493-133,468,092 , LEAP2, 395 more genes
    nsv4675472copy number variation1nstd102humanLikely pathogenic GRCh37 chr5: 87,792,844-109,221,844 , GRCh38.p12 chr5: 88,497,027-109,886,143 CAST, CETN3, 202 more genes
    nsv4455983copy number variation1nstd102humanPathogenic GRCh37 chr5: 89,949,118-129,317,455 , GRCh38.p12 chr5: 90,653,301-129,981,762 LOC345576, LOC107986436, 419 more genes
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