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Items: 1 to 20 of 23

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4681073copy number variation1nstd102humanPathogenic GRCh37 chr11: 72,083,949-72,091,448 , GRCh38.p12 chr11: 72,372,905-72,380,404 CLPB
    nsv7094188copy number variation1nstd102humanPathogenic GRCh37 chr11: 72,145,398-72,150,823 , GRCh38.p12 chr11: 72,434,354-72,439,779 CLPB
    nsv7094184copy number variation1nstd102humanPathogenic GRCh37 chr11: 72,004,411-72,006,712 , GRCh38.p12 chr11: 72,293,367-72,295,668 CLPB
    nsv6309287copy number variation1nstd102humanPathogenic GRCh37 chr11: 72,145,096-72,145,518 , GRCh38.p12 chr11: 72,434,052-72,434,474 CLPB
    nsv7094187copy number variation1nstd102humanPathogenic GRCh37 chr11: 72,145,398-72,145,517 , GRCh38.p12 chr11: 72,434,354-72,434,473 CLPB
    nsv7094185copy number variation1nstd102humanLikely pathogenic GRCh37 chr11: 72,083,996-72,087,051 , GRCh38.p12 chr11: 72,372,952-72,376,007 CLPB
    nsv5380958copy number variation1nstd102humanUncertain significance GRCh37 chr11: 72,083,949-72,084,078 , GRCh38.p12 chr11: 72,372,905-72,373,034 CLPB
    nsv7094015copy number variation1nstd102humanUncertain significance GRCh37 chr11: 72,141,336-72,145,518 , GRCh38.p12 chr11: 72,430,292-72,434,474 CLPB
    nsv4450493copy number variation1nstd102humanPathogenic GRCh37 chr11: 72,004,391-72,145,538 , GRCh38 chr11: 72,293,347-72,434,494 CLPB, LOC112268077
    nsv7093946copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,903,218-72,019,668 , GRCh38.p12 chr11: 72,192,174-72,308,624 CLPB, PHOX2A, 5 more genes
    nsv5380796copy number variation1nstd102humanPathogenic GRCh37 chr11: 11,835,569-118,373,112 , GRCh38.p12 chr11: 11,814,022-118,502,397 CLPB, FAUP4, 2031 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 CLPB, TPBGL, 173 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 CLPB, RN7SL786P, 146 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 CLPB, OR7E128P, 68 more genes
    nsv3893233copy number variation1nstd102humanPathogenic GRCh37 chr11: 70,864-134,938,470 , GRCh38.p12 chr11: 70,864-135,068,576 CLPB, LOC105376598, 2842 more genes
    nsv3900144copy number variation1nstd102humanPathogenic GRCh37 chr11: 198,510-134,934,063 , GRCh38.p12 chr11: 198,510-135,064,169 CLPB, RTN3, 2833 more genes
    nsv3908873copy number variation2nstd102humanPathogenic GRCh37 chr11: 230,616-134,938,470 , GRCh38.p12 chr11: 230,616-135,068,576 CLPB, IGHMBP2, 2829 more genes
    nsv6315537copy number variation1nstd102humanPathogenic GRCh37 chr11: 32,799,481-134,938,470 , GRCh38.p12 chr11: 32,777,935-135,068,576 CLPB, PYGM, 2125 more genes
    nsv3898361copy number variation1nstd102humanPathogenic GRCh37 chr11: 71,588,805-116,680,918 , GRCh38.p12 chr11: 71,877,759-116,810,202 CLPB, SESN3, 694 more genes
    nsv6314007copy number variation1nstd102humanUncertain significance GRCh37 chr11: 71,567,724-72,488,649 , GRCh38.p12 chr11: 71,856,678-72,777,604 CLPB, STARD10, 38 more genes
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