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Items: 1 to 20 of 48042

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5380706translocation1nstd200human GRCh38 chr2: 211,546,989-211,546,989 , GRCh38 chr2: 211,543,617-211,543,617 , GRCh37.p13 chr2: 212,411,714-212,411,714 , GRCh37.p13 chr2: 212,408,342-212,408,342 ERBB4
    nsv5380700translocation1nstd200human GRCh38 chr2: 147,957,121-147,957,121 , GRCh38 chr2: 147,953,216-147,953,216 , GRCh37.p13 chr2: 148,710,785-148,710,785 , GRCh37.p13 chr2: 148,714,690-148,714,690 ORC4
    nsv5380696translocation1nstd200human GRCh38 chr2: 144,315,329-144,315,329 , GRCh38 chr2: 144,316,208-144,316,208 , GRCh37.p13 chr2: 145,072,896-145,072,896 , GRCh37.p13 chr2: 145,073,775-145,073,775 GTDC1
    nsv5380695translocation1nstd200human GRCh38 chr2: 144,316,572-144,316,572 , GRCh38 chr2: 144,315,322-144,315,322 , GRCh37.p13 chr2: 145,074,139-145,074,139 , GRCh37.p13 chr2: 145,072,889-145,072,889 GTDC1
    nsv5380694translocation1nstd200human GRCh38 chr2: 143,315,903-143,315,903 , GRCh38 chr2: 143,314,762-143,314,762 , GRCh37.p13 chr2: 144,072,331-144,072,331 , GRCh37.p13 chr2: 144,073,472-144,073,472 ARHGAP15
    nsv5380693translocation1nstd200human GRCh38 chr2: 143,316,598-143,316,598 , GRCh38 chr2: 143,314,758-143,314,758 , GRCh37.p13 chr2: 144,072,327-144,072,327 , GRCh37.p13 chr2: 144,074,167-144,074,167 ARHGAP15
    nsv5380690translocation1nstd200human GRCh38 chr2: 143,237,691-143,237,691 , GRCh38 chr2: 143,240,846-143,240,846 , GRCh37.p13 chr2: 143,995,260-143,995,260 , GRCh37.p13 chr2: 143,998,415-143,998,415 ARHGAP15
    nsv5380689translocation1nstd200human GRCh38 chr2: 143,237,857-143,237,857 , GRCh38 chr2: 143,231,141-143,231,141 , GRCh37.p13 chr2: 143,988,710-143,988,710 , GRCh37.p13 chr2: 143,995,426-143,995,426 ARHGAP15
    nsv5380686translocation1nstd200human GRCh38 chr1: 32,006,917-32,006,917 , GRCh38 chr1: 32,012,288-32,012,288 , GRCh37.p13 chr1: 32,472,518-32,472,518 , GRCh37.p13 chr1: 32,477,889-32,477,889 KHDRBS1
    nsv5380685translocation1nstd200human GRCh38 chr2: 140,748,716-140,748,716 , GRCh38 chr2: 140,748,846-140,748,846 , GRCh37.p13 chr2: 141,506,415-141,506,415 , GRCh37.p13 chr2: 141,506,285-141,506,285 LRP1B
    nsv5380679translocation1nstd200human GRCh38 chr2: 137,194,869-137,194,869 , GRCh38 chr2: 137,245,274-137,245,274 , GRCh37.p13 chr2: 138,002,844-138,002,844 , GRCh37.p13 chr2: 137,952,439-137,952,439 THSD7B
    nsv5380678translocation1nstd200human GRCh38 chr2: 137,193,504-137,193,504 , GRCh38 chr2: 137,197,154-137,197,154 , GRCh37.p13 chr2: 137,954,724-137,954,724 , GRCh37.p13 chr2: 137,951,074-137,951,074 THSD7B
    nsv5380676translocation1nstd200human GRCh38 chr2: 136,086,848-136,086,848 , GRCh38 chr2: 136,087,642-136,087,642 , GRCh37.p13 chr2: 136,845,212-136,845,212 , GRCh37.p13 chr2: 136,844,418-136,844,418
    nsv5380674translocation1nstd200human GRCh38 chr2: 133,452,460-133,452,460 , GRCh38 chr2: 133,453,749-133,453,749 , GRCh37.p13 chr2: 134,210,031-134,210,031 , GRCh37.p13 chr2: 134,211,320-134,211,320 NCKAP5
    nsv5380673translocation1nstd200human GRCh38 chr2: 133,448,776-133,448,776 , GRCh38 chr2: 133,452,963-133,452,963 , GRCh37.p13 chr2: 134,206,347-134,206,347 , GRCh37.p13 chr2: 134,210,534-134,210,534 NCKAP5
    nsv5380670translocation1nstd200human GRCh38 chr2: 132,762,248-132,762,248 , GRCh38 chr2: 132,761,172-132,761,172 , GRCh37.p13 chr2: 133,519,821-133,519,821 , GRCh37.p13 chr2: 133,518,745-133,518,745 NCKAP5
    nsv5380669translocation1nstd200human GRCh38 chr2: 132,762,252-132,762,252 , GRCh38 chr2: 132,760,650-132,760,650 , GRCh37.p13 chr2: 133,518,223-133,518,223 , GRCh37.p13 chr2: 133,519,825-133,519,825 NCKAP5
    nsv5380666translocation1nstd200human GRCh38 chr2: 203,917,246-203,917,246 , GRCh38 chr2: 132,036,464-132,036,464 , GRCh37.p13 chr2: 204,781,969-204,781,969 , GRCh37.p13 chr2: 132,794,037-132,794,037 LINC01945
    nsv5380663translocation1nstd200human GRCh38 chr2: 130,132,631-130,132,631 , GRCh38 chr2: 131,206,355-131,206,355 , GRCh37.p13 chr2: 131,963,928-131,963,928 , GRCh37.p13 chr2: 130,890,204-130,890,204 MED15P9
    nsv5380659translocation1nstd200human GRCh38 chr2: 129,797,971-129,797,971 , GRCh38 chr2: 129,787,275-129,787,275 , GRCh37.p13 chr2: 130,544,848-130,544,848 , GRCh37.p13 chr2: 130,555,544-130,555,544 LOC107985945
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