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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3161762copy number variation1nstd151human GRCh37 (hg19) chr17: 42,030,321-42,117,629 , GRCh38 (hg38) chr17: 43,952,953-44,040,261 LSM12, NAGS, 2 more genes
    esv4010335copy number variation1estd233human GRCh37 (hg19) chr17: 41,468,000-43,513,000 , GRCh38 (hg38) chr17: 43,390,632-45,435,634 MAP3K14-AS1, HDAC5, 61 more genes
    nsv2777361copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr17: 31,824,931-78,654,742 , GRCh37 (hg19) chr17: 34,750,818-81,048,189 , GRCh38 (hg38) chr17: 36,321,896-83,103,577 SNORA38B, MAPT-AS1, 897 more genes
    nsv2774357copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr17: 16,698,288-78,654,742 , GRCh37 (hg19) chr17: 16,757,563-81,048,189 , GRCh38 (hg38) chr17: 16,854,249-83,103,577 SNORA38B, MIR365B, 1150 more genes
    nsv2773787copy number variation1nstd37humanUncertain significance NCBI36 (hg18) chr17: 39,298,066-39,477,792 , GRCh37 (hg19) chr17: 41,942,540-42,122,266 , GRCh38 (hg38) chr17: 43,865,172-44,044,898 LINC01976, LSM12, 6 more genes
    nsv2769779copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr17: 526-81,041,938 , GRCh38 (hg38) chr17: 150,733-83,084,062 , NCBI36 (hg18) chr17: 526-78,635,227 SNORA38B, MIR744, 1495 more genes
    esv3879709copy number variation2estd219human GRCh37 (hg19) chr17: 42,122,248-42,124,862 , GRCh38 (hg38) chr17: 44,044,880-44,047,494 LSM12
    nsv1875761short tandem repeat1nstd128human GRCh37 (hg19) chr17: 42,143,971-42,143,991 , GRCh38 (hg38) chr17: 44,066,603-44,066,623 LSM12
    nsv1875760short tandem repeat2nstd128human GRCh37 (hg19) chr17: 42,134,516-42,134,535 , GRCh38 (hg38) chr17: 44,057,148-44,057,167 LSM12
    nsv1875759short tandem repeat14nstd128human GRCh37 (hg19) chr17: 42,125,387-42,125,432 , GRCh38 (hg38) chr17: 44,048,019-44,048,064 LSM12
    nsv1875757short tandem repeat2nstd128human GRCh37 (hg19) chr17: 42,117,818-42,117,832 , GRCh38 (hg38) chr17: 44,040,450-44,040,464 LSM12
    nsv1875186short tandem repeat3nstd128human GRCh37 (hg19) chr17: 42,140,274-42,140,287 , GRCh38 (hg38) chr17: 44,062,906-44,062,919 LSM12
    nsv1875185short tandem repeat1nstd128human GRCh37 (hg19) chr17: 42,136,548-42,136,575 , GRCh38 (hg38) chr17: 44,059,180-44,059,207 LSM12
    nsv1875184short tandem repeat2nstd128human GRCh37 (hg19) chr17: 42,135,142-42,135,166 , GRCh38 (hg38) chr17: 44,057,774-44,057,798 LSM12
    nsv1875183short tandem repeat2nstd128human GRCh37 (hg19) chr17: 42,130,209-42,130,223 , GRCh38 (hg38) chr17: 44,052,841-44,052,855 LSM12
    nsv1875182short tandem repeat16nstd128human GRCh37 (hg19) chr17: 42,118,642-42,118,655 , GRCh38 (hg38) chr17: 44,041,274-44,041,287 LSM12
    nsv1875181short tandem repeat1nstd128human GRCh37 (hg19) chr17: 42,118,348-42,118,376 , GRCh38 (hg38) chr17: 44,040,980-44,041,008 LSM12
    nsv1874524short tandem repeat1nstd128human GRCh37 (hg19) chr17: 42,144,669-42,144,687 , GRCh38 (hg38) chr17: 44,067,301-44,067,319 LSM12
    nsv1874523short tandem repeat3nstd128human GRCh37 (hg19) chr17: 42,135,613-42,135,643 , GRCh38 (hg38) chr17: 44,058,245-44,058,275 LSM12
    nsv1874522short tandem repeat1nstd128human GRCh37 (hg19) chr17: 42,130,270-42,130,286 , GRCh38 (hg38) chr17: 44,052,902-44,052,918 LSM12
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