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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3870819copy number variation1nstd102humannot provided GRCh38 chr14: 90,292,547-90,335,706 , GRCh37 chr14: 90,758,891-90,802,050 NRDE2
    nsv3889099copy number variation4nstd102humannot provided GRCh38 chr14: 90,322,590-90,335,706 , GRCh37 chr14: 90,788,934-90,802,050 NRDE2
    esv3648728copy number variation1estd216humannot provided GRCh38.p12 chr14: 90,292,547-90,335,706 , GRCh37 chr14: 90,758,891-90,802,050 NRDE2
    esv3648732copy number variation1estd216humannot provided GRCh38.p12 chr14: 90,322,590-90,335,706 , GRCh37 chr14: 90,788,934-90,802,050 NRDE2
    esv3648731copy number variation1estd216humannot provided GRCh38.p12 chr14: 90,322,590-90,335,706 , GRCh37 chr14: 90,788,934-90,802,050 NRDE2
    esv3648730copy number variation1estd216humannot provided GRCh38.p12 chr14: 90,322,590-90,335,706 , GRCh37 chr14: 90,788,934-90,802,050 NRDE2
    esv3648729copy number variation1estd216humannot provided GRCh38.p12 chr14: 90,322,590-90,335,706 , GRCh37 chr14: 90,788,934-90,802,050 NRDE2
    nsv3893892copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,783,137-96,908,198 , GRCh38.p12 chr14: 84,316,793-96,441,861 NRDE2, DICER1, 175 more genes
    nsv4675107copy number variation1nstd102humanPathogenic GRCh37 chr14: 84,783,523-96,907,490 , GRCh38.p12 chr14: 84,317,179-96,441,153 NRDE2, SHLD2P2, 175 more genes
    nsv6314190copy number variation1nstd102humanPathogenic GRCh37 chr14: 88,345,625-94,773,741 , GRCh38.p12 chr14: 87,879,281-94,140,555 NRDE2, EML5, 104 more genes
    nsv7137135copy number variation1nstd102humanPathogenic GRCh37 chr14: 88,401,076-94,725,706 , GRCh38.p12 chr14: 87,934,732-94,140,555 NRDE2, LOC100128939, 104 more genes
    nsv3922566copy number variation1nstd102humanPathogenic GRCh38 chr14: 90,255,156-95,274,696 , GRCh37 chr14: 90,721,500-95,741,033 , NCBI36 chr14: 89,791,253-94,810,786 NRDE2, RPSAP4, 97 more genes
    nsv3902883copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,000,422-107,289,053 , GRCh38.p12 chr14: 18,223,945-106,880,863 NRDE2, LOC440181, 1998 more genes
    nsv3907460copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,280,733-107,287,663 , GRCh38.p12 chr14: 18,504,256-106,879,456 NRDE2, BANF1P1, 1996 more genes
    nsv3899639copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,327,823-107,287,663 , GRCh38.p12 chr14: 18,551,346-106,879,456 NRDE2, LOC100289511, 1996 more genes
    nsv3903256copy number variation1nstd102humanPathogenic GRCh37 chr14: 19,794,561-107,234,280 , GRCh38.p12 chr14: 19,652,445-106,826,050 NRDE2, DHRS7, 1946 more genes
    nsv3919106copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38 chr14: 20,043,514-106,877,229 , NCBI36 chr14: 19,581,513-106,356,482 NRDE2, SRMP2, 1929 more genes
    nsv3904265copy number variation1nstd102humanPathogenic GRCh37 chr14: 20,511,673-107,285,437 , GRCh38.p12 chr14: 20,043,514-106,877,229 NRDE2, CRIP1, 1929 more genes
    nsv3917422copy number variation1nstd102humanPathogenic GRCh38 chr14: 20,151,149-106,855,263 , NCBI36 chr14: 19,689,148-106,334,523 , GRCh37 chr14: 20,619,308-107,263,478 NRDE2, MIR656, 1918 more genes
    nsv6315524copy number variation1nstd102humanPathogenic GRCh37 chr14: 37,671,058-106,985,955 , GRCh38.p12 chr14: 37,201,853-106,530,013 NRDE2, PAPOLA-DT, 1338 more genes
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