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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3890090copy number variation1nstd102humanBenign GRCh37 chr8: 146,142,510-146,166,217 , GRCh38.p12 chr8: 144,917,125-144,940,831 ZNF16
    nsv3892267copy number variation1nstd102humanBenign GRCh37 chr8: 146,171,994-146,175,137 , GRCh38.p12 chr8: 144,946,608-144,949,751 ZNF16
    nsv3894440copy number variation1nstd102humanBenign GRCh37 chr8: 146,171,994-146,173,636 , GRCh38.p12 chr8: 144,946,608-144,948,250 ZNF16
    nsv3893103copy number variation1nstd102humanBenign GRCh37 chr8: 146,171,994-146,172,751 , GRCh38.p12 chr8: 144,946,608-144,947,365 ZNF16
    nsv3917354copy number variation1nstd102humanUncertain significance NCBI36 chr8: 146,099,529-146,164,704 , GRCh37.p13 chr8: 146,128,725-146,193,900 , GRCh38.p12 chr8: 144,903,340-144,968,514 ZNF16
    nsv3916736copy number variation1nstd102humanUncertain significance NCBI36 chr8: 146,122,289-146,168,432 , GRCh37.p13 chr8: 146,151,485-146,197,628 , GRCh38.p12 chr8: 144,926,099-144,972,242 ZNF16, ZNF252P
    nsv3897455copy number variation1nstd102humanBenign GRCh37 chr8: 146,159,770-146,245,372 , GRCh38.p12 chr8: 144,934,384-145,019,986 ZNF16, ZNF252P, 2 more genes
    nsv3912271copy number variation1nstd102humanBenign NCBI36 chr8: 146,131,843-146,245,639 , GRCh37 chr8: 146,161,039-146,274,835 , GRCh38 chr8: 144,935,653-145,049,449 ZNF16, ZNF252P-AS1, 3 more genes
    nsv3904872copy number variation1nstd102humanBenign GRCh37 chr8: 146,151,479-146,245,372 , GRCh38.p12 chr8: 144,926,093-145,019,986 ZNF16, ZNF252P-AS1, 2 more genes
    nsv3912848copy number variation1nstd102humanLikely benign GRCh37 chr8: 146,151,358-146,235,425 , NCBI36 chr8: 146,122,162-146,206,229 , GRCh38 chr8: 144,925,972-145,010,039 ZNF16, ZNF252P, 2 more genes
    nsv3894482copy number variation1nstd102humanLikely benign GRCh37 chr8: 146,157,876-146,231,912 , GRCh38.p12 chr8: 144,932,490-145,006,526 ZNF16, ZNF252P-AS1, 2 more genes
    nsv3923566copy number variation1nstd102humanUncertain significance NCBI36 chr8: 146,147,210-146,197,836 , GRCh37.p13 chr8: 146,176,406-146,227,032 , GRCh38.p12 chr8: 144,951,020-145,001,646 ZNF16, ZNF252P, 2 more genes
    nsv3915173copy number variation1nstd102humanPathogenic NCBI36 chr8: 3,938-146,274,826 , GRCh37.p13 chr8: 13,938-146,304,022 , GRCh38.p12 chr8: 63,938-145,078,636 ZNF16, RN7SL474P, 2109 more genes
    nsv3901821copy number variation1nstd102humanPathogenic GRCh37 chr8: 10,213-146,293,414 , GRCh38.p12 chr8: 60,213-145,068,028 ZNF16, TBC1D31, 2109 more genes
    nsv4349554copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38.p12 chr8: 208,048-145,070,385 ZNF16, LOC101929488, 2105 more genes
    nsv3916777copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,048-146,295,771 , GRCh38 chr8: 208,048-145,070,385 , NCBI36 chr8: 148,048-146,266,575 ZNF16, RPL5P22, 2105 more genes
    nsv3898123copy number variation2nstd102humanPathogenic GRCh37 chr8: 158,049-146,295,771 , GRCh38.p12 chr8: 208,049-145,070,385 ZNF16, SPAG1, 2105 more genes
    nsv3908608copy number variation1nstd102humanPathogenic GRCh37 chr8: 164,984-146,293,414 , GRCh38.p12 chr8: 214,984-145,068,028 ZNF16, LINC01617, 2105 more genes
    nsv3893757copy number variation1nstd102humanPathogenic GRCh37 chr8: 158,991-146,280,828 , GRCh38.p12 chr8: 208,991-145,055,442 ZNF16, LOC105375890, 2105 more genes
    nsv3923310copy number variation1nstd102humanPathogenic NCBI36 chr8: 166,452-146,264,902 , GRCh38 chr8: 226,452-145,068,712 , GRCh37 chr8: 176,452-146,294,098 ZNF16, LOC112268023, 2105 more genes
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