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Items: 1 to 20 of 127

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5916515copy number variation1nstd209human GRCh38 chr11: 72,772,206-72,772,396 , GRCh37.p13 chr11: 72,483,251-72,483,441 STARD10
    nsv5505212copy number variation1nstd206human GRCh38 chr11: 72,788,947-72,789,359 , GRCh37.p13 chr11: 72,499,992-72,500,404 STARD10
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 FAUP4, MMP7, 2031 more genes
    nsv5355357translocation1nstd200human GRCh38 chr11: 72,788,947-72,788,947 , GRCh38 chr11: 72,789,359-72,789,359 , GRCh37.p13 chr11: 72,499,992-72,499,992 , GRCh37.p13 chr11: 72,500,404-72,500,404 STARD10
    nsv5318755copy number variation1nstd204human GRCh38.p13 chr11: 72,788,944-72,789,368 , GRCh37.p13 chr11: 72,499,989-72,500,413 STARD10
    nsv5125224mobile element insertion1nstd203human GRCh38 chr11: 72,761,901-72,761,942 , GRCh37.p13 chr11: 72,472,946-72,472,987 STARD10
    nsv5120167mobile element insertion1nstd203human GRCh38 chr11: 72,757,145-72,757,158 , GRCh37.p13 chr11: 72,468,190-72,468,203 STARD10
    nsv4987264copy number variation1nstd200human GRCh38 chr11: 72,756,498-72,757,232 , GRCh37.p13 chr11: 72,467,543-72,468,277 STARD10
    nsv4846786copy number variation1nstd200human GRCh37 chr11: 72,499,992-72,500,404 , GRCh38.p12 chr11: 72,788,947-72,789,359 STARD10
    nsv4713821copy number variation1nstd195human GRCh37 chr11: 72,354,901-72,655,251 , GRCh38.p12 chr11: 72,643,857-72,944,206 , ARAP1-AS2, 11 more genes
    nsv3919985copy number variation1nstd102humanPathogenic NCBI36 chr11: 70,668,528-72,528,680 , GRCh37.p13 chr11: 70,990,880-72,851,032 , GRCh38.p12 chr11: 71,279,834-73,139,987 OR7E128P, OR7E87P, 68 more genes
    nsv3916301copy number variation1nstd102humanPathogenic GRCh38 chr11: 71,928,796-77,064,521 , GRCh37 chr11: 71,639,842-76,751,808 , NCBI36 chr11: 71,317,490-76,453,216 RN7SL786P, LIPT2-AS1, 146 more genes
    nsv3915804copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,680,927-77,943,941 , NCBI36 chr11: 71,358,575-77,621,589 , GRCh38 chr11: 71,969,881-78,232,895 TPBGL, MAP6, 173 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 IGHMBP2, SYTL2, 2829 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 RTN3, KRTAP5-13P, 2833 more genes
    nsv3898361copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202 SESN3, LOC107984352, 694 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 LOC105376598, OSBPL9P2, 2842 more genes
    nsv3232205insertion1nstd152human GRCh38 chr11: 72,749,663-72,766,413 , GRCh37.p13 chr11: 72,460,708-72,477,458 ARAP1, STARD10
    nsv3157882copy number variation1nstd151human GRCh37 chr11: 72,423,238-72,469,683 , GRCh38.p12 chr11: 72,712,193-72,758,638 ARAP1, STARD10
    nsv3156628copy number variation1nstd151human GRCh37 chr11: 72,413,947-72,492,231 , GRCh38.p12 chr11: 72,702,902-72,781,186 ARAP1-AS2, ARAP1, 2 more genes
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