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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    esv3156872copy number variation1estd209human GRCh37 chr11: 124,609,567-124,609,573 , GRCh38.p12 chr11: 124,739,671-124,739,677 NRGN
    esv2213859insertion1estd194human NCBI36 chr11: 124,115,222-124,115,222 , GRCh37.p13 chr11: 124,610,012-124,610,012 , GRCh38.p12 chr11: 124,740,116-124,740,116 NRGN
    esv1730518insertion1estd22human NCBI36 chr11: 124,119,019-124,119,019 , GRCh37.p13 chr11: 124,613,809-124,613,809 , GRCh38.p12 chr11: 124,743,913-124,743,913 NRGN
    nsv1617400short tandem repeat1nstd128human GRCh37 chr11: 124,614,692-124,614,726 , GRCh38.p12 chr11: 124,744,796-124,744,830 NRGN
    nsv1618884short tandem repeat12nstd128human GRCh37 chr11: 124,613,794-124,613,809 , GRCh38.p12 chr11: 124,743,898-124,743,913 NRGN
    nsv1623876short tandem repeat1nstd128human GRCh37 chr11: 124,612,392-124,612,403 , GRCh38.p12 chr11: 124,742,496-124,742,507 NRGN
    nsv952751copy number variation1nstd73human GRCh37 chr11: 124,614,701-124,618,700 , GRCh38.p12 chr11: 124,744,805-124,748,804 NRGN, VSIG2
    nsv898438copy number variation1nstd71human NCBI36 chr11: 124,117,369-124,141,583 , GRCh37.p13 chr11: 124,612,159-124,636,373 , GRCh38.p12 chr11: 124,742,263-124,766,477 NRGN, MSANTD2, 3 more genes
    nsv556487copy number variation1nstd54human NCBI36 chr11: 124,105,968-124,140,354 , GRCh37.p13 chr11: 124,600,758-124,635,144 , GRCh38.p12 chr11: 124,730,862-124,765,248 NRGN, LOC101929340, 3 more genes
    esv3865830copy number variation1estd219human GRCh37 chr11: 124,610,196-124,622,345 , GRCh38.p12 chr11: 124,740,300-124,752,449 NRGN, ESAM, 1 more genes
    esv3627986copy number variation1estd214human GRCh37 chr11: 124,610,196-124,622,345 , GRCh38.p12 chr11: 124,740,300-124,752,449 NRGN, VSIG2, 1 more genes
    nsv4353314copy number variation1nstd102humanPathogenic NCBI36 chr11: 118,590,952-134,373,758 , GRCh37.p13 chr11: 119,085,742-134,868,548 , GRCh38.p12 chr11: 119,215,032-134,998,654 NRGN, RPL34P21, 319 more genes
    nsv4354265copy number variation1nstd102humanPathogenic NCBI36 chr11: 118,800,217-134,450,377 , GRCh37.p13 chr11: 119,295,007-134,945,165 , GRCh38.p12 chr11: 119,424,297-135,075,271 NRGN, POU2F3, 312 more genes
    nsv4359864copy number variation1nstd102humanPathogenic NCBI36 chr11: 118,809,829-134,373,617 , GRCh37.p13 chr11: 119,304,619-134,868,407 , GRCh38.p12 chr11: 119,433,909-134,998,513 NRGN, FLI1, 309 more genes
    nsv3891077copy number variation1nstd102humanPathogenic GRCh37 chr11: 119,513,909-134,938,470 , GRCh38.p12 chr11: 119,643,199-135,068,576 NRGN, B3GAT1, 305 more genes
    nsv3906843copy number variation1nstd102humanPathogenic GRCh37 chr11: 119,538,664-134,938,470 , GRCh38.p12 chr11: 119,667,954-135,068,576 NRGN, OR8B3, 304 more genes
    nsv3902675copy number variation1nstd102humanPathogenic GRCh37 chr11: 119,807,473-134,868,407 , GRCh38.p12 chr11: 119,936,764-134,998,513 NRGN, SNX19, 299 more genes
    nsv4356479copy number variation1nstd102humanPathogenic NCBI36 chr11: 119,891,678-134,450,377 , GRCh37.p13 chr11: 120,386,468-134,945,165 , GRCh38.p12 chr11: 120,515,759-135,075,271 NRGN, OR8B7P, 287 more genes
    nsv3901752copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,527,021-134,938,470 , GRCh38.p12 chr11: 120,656,312-135,068,576 NRGN, OR8A2P, 284 more genes
    nsv4436748copy number variation1nstd102humanPathogenic GRCh37 chr11: 120,576,984-134,934,063 , GRCh38.p12 chr11: 120,706,275-135,064,169 NRGN, SNORD153, 284 more genes
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