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Items: 1 to 20 of 131

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5970839inversion1nstd209human GRCh38 chr11: 74,527,352-75,035,369 , GRCh37.p13 chr11: 74,238,397-74,746,414 SPCS2, POLD3, 14 more genes
    nsv5709143mobile element insertion1nstd211human GRCh38 chr11: 74,960,831-74,960,831 , GRCh37.p13 chr11: 74,671,876-74,671,876 SPCS2
    nsv5599480copy number variation1nstd207human GRCh38 chr11: 74,948,182-74,948,342 , GRCh37.p13 chr11: 74,659,227-74,659,387 SPCS2, XRRA1
    nsv5406409mobile element insertion1nstd206human GRCh38 chr11: 74,960,831-74,960,882 , GRCh37.p13 chr11: 74,671,876-74,671,927 SPCS2
    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
    nsv4987323copy number variation1nstd200human GRCh38 chr11: 74,956,304-74,958,524 , GRCh37.p13 chr11: 74,667,349-74,669,569 SPCS2
    nsv4834333copy number variation1nstd200human GRCh37 chr11: 74,660,955-74,661,408 , GRCh38.p12 chr11: 74,949,910-74,950,363 SPCS2
    nsv4600771copy number variation1nstd183human GRCh37 chr11: 74,648,116-74,781,671 , GRCh38.p12 chr11: 74,937,071-75,070,626 SPCS2, NEU3, 4 more genes
    nsv4479647mobile element insertion1nstd166human GRCh37.p13 chr11: 74,667,055-74,667,055 , GRCh38.p12 chr11: 74,956,010-74,956,010 SPCS2
    nsv4195088copy number variation1nstd166human GRCh37.p13 chr11: 74,677,626-74,677,830 , GRCh38.p12 chr11: 74,966,581-74,966,785 SPCS2, RNU6-216P
    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
    nsv3153385copy number variation1nstd151human GRCh37 chr11: 74,660,329-74,660,447 , GRCh38.p12 chr11: 74,949,284-74,949,402 SPCS2, XRRA1
    nsv3144312copy number variation1nstd151human GRCh37 chr11: 74,574,024-74,800,763 , GRCh38.p12 chr11: 74,862,979-75,089,718 NPM1P50, RNU6-216P, 7 more genes
    nsv3142968copy number variation1nstd151human GRCh37 chr11: 74,676,806-76,893,648 , GRCh38.p12 chr11: 74,965,761-77,182,603 , LOC107984358, 56 more genes
    esv4009164inversion1estd231human GRCh37 chr11: 74,238,397-74,746,415 , GRCh38.p12 chr11: 74,527,352-75,035,370 SPCS2, POLD3, 14 more genes
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