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Items: 1 to 20 of 221

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7148241copy number variation1nstd102humanPathogenic GRCh38 chr4: 79,123,548-99,457,773 , GRCh37.p13 chr4: 80,044,702-100,378,930 LOC105377327, LOC105377324, 214 more genes
    nsv7054609inversion1nstd229human GRCh38 chr4: 95,257,712-104,152,159 , GRCh37.p13 chr4: 96,178,863-105,073,316 SLC39A8, PABPC1P7, 96 more genes
    nsv7052845inversion1nstd229human GRCh38 chr4: 97,450,222-102,053,198 , GRCh37.p13 chr4: 98,371,373-102,974,355 RNU6-462P, LOC105377345, 58 more genes
    nsv7052661inversion1nstd229human GRCh38 chr4: 96,912,053-103,991,076 , GRCh37.p13 chr4: 97,833,204-104,912,233 MIR1255A, LOC107986297, 86 more genes
    nsv7046928inversion1nstd229human GRCh38 chr4: 95,051,434-103,882,549 , GRCh37.p13 chr4: 95,972,585-104,803,706 PABPC1P7, RN7SL728P, 95 more genes
    nsv7044544inversion1nstd229human GRCh38 chr4: 98,964,941-108,185,877 , GRCh37.p13 chr4: 99,886,092-109,107,033 LOC102725220, TACR3, 117 more genes
    nsv6754642copy number variation1nstd229human GRCh38 chr4: 99,102,725-99,212,334 , GRCh37.p13 chr4: 100,023,876-100,133,491 LOC100507053, ADH6, 3 more genes
    nsv6751008copy number variation1nstd229human GRCh38 chr4: 99,113,001-99,123,300 , GRCh37.p13 chr4: 100,034,152-100,044,451 LOC100507053, ADH4
    nsv6750890copy number variation1nstd229human GRCh38 chr4: 99,064,601-99,205,500 , GRCh37.p13 chr4: 99,985,752-100,126,657 ADH5, PCNAP1, 4 more genes
    nsv6740025copy number variation1nstd229human GRCh38 chr4: 99,026,449-99,231,369 , GRCh37.p13 chr4: 99,947,600-100,152,526 PCNAP2, ADH6, 5 more genes
    nsv6636966copy number variation1nstd102humanUncertain significance GRCh37 chr4: 99,918,661-100,046,008 , GRCh38.p12 chr4: 98,997,510-99,124,857 ADH5, METAP1, 4 more genes
    nsv6634780copy number variation1nstd227human GRCh38.p12 chr4: 99,121,258-99,122,133 , GRCh37 chr4: 100,042,409-100,043,284 ADH4, LOC100507053
    nsv6630192copy number variation1nstd224human GRCh37 chr4: 99,863,585-100,335,586 , GRCh38.p12 chr4: 98,942,434-99,414,429 ADH1B, ADH5, 15 more genes
    nsv6629271copy number variation1nstd224human GRCh37 chr4: 100,042,262-100,131,746 , GRCh38.p12 chr4: 99,121,111-99,210,589 PCNAP1, ADH4, 3 more genes
    nsv6563046inversion1nstd223human GRCh38 chr4: 99,128,332-99,128,825 , GRCh37.p13 chr4: 100,049,483-100,049,976 LOC100507053, ADH4
    nsv6560198inversion1nstd223human GRCh38 chr4: 99,122,057-99,123,007 , GRCh37.p13 chr4: 100,043,208-100,044,158 LOC100507053, ADH4
    nsv6393120copy number variation1nstd223human GRCh38 chr4: 99,127,259-99,130,477 , GRCh37.p13 chr4: 100,048,410-100,051,628 LOC100507053, ADH4
    nsv6378653copy number variation1nstd223human GRCh38 chr4: 99,132,889-99,133,402 , GRCh37.p13 chr4: 100,054,040-100,054,553 ADH4, LOC100507053
    nsv6313762copy number variation1nstd102humanUncertain significance GRCh37 chr4: 99,835,828-100,089,147 , GRCh38.p12 chr4: 98,914,677-99,167,990 PCNAP2, RNU7-149P, 10 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
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