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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv4681299copy number variation1nstd102humanLikely pathogenic GRCh37 chr12: 936,198-971,446 , GRCh38.p12 chr12: 827,032-862,280 WNK1
    nsv3899826copy number variation1nstd102humanBenign GRCh37 chr12: 857,501-874,764 , GRCh38.p12 chr12: 748,335-765,598 WNK1
    nsv3909368copy number variation1nstd102humanBenign GRCh37 chr12: 863,177-874,764 , GRCh38.p12 chr12: 754,011-765,598 WNK1
    nsv3906368copy number variation1nstd102humanBenign GRCh37 chr12: 863,517-873,411 , GRCh38.p12 chr12: 754,351-764,245 WNK1
    nsv3897809copy number variation1nstd102humanBenign GRCh37 chr12: 866,857-876,288 , GRCh38.p12 chr12: 757,691-767,122 WNK1
    nsv7094229copy number variation1nstd102humanUncertain significance GRCh37 chr12: 922,788-1,017,958 , GRCh38.p12 chr12: 813,622-908,792 WNK1
    nsv4682372copy number variation1nstd102humanUncertain significance GRCh37 chr12: 936,198-1,017,968 , GRCh38.p12 chr12: 827,032-908,802 WNK1
    nsv4681650copy number variation1nstd102humanUncertain significance GRCh37 chr12: 987,368-1,017,968 , GRCh38.p12 chr12: 878,202-908,802 WNK1
    nsv6309329copy number variation1nstd102humanUncertain significance GRCh37 chr12: 990,838-1,017,958 , GRCh38.p12 chr12: 881,672-908,792 WNK1
    nsv7096581copy number variation1nstd102humanUncertain significance GRCh37 chr2: 167,160,728-167,168,266 , GRCh38.p12 chr2: 166,304,218-166,311,756 SCN9A
    nsv7095869copy number variation1nstd102humanPathogenic GRCh37 chr2: 167,085,181-167,168,266 , GRCh38.p12 chr2: 166,228,671-166,311,756 SCN9A, SCN1A-AS1
    nsv3877799copy number variation1nstd102humanPathogenic GRCh38 chr12: 766,596-807,868 , GRCh37 chr12: 875,762-917,034 WNK1, RNU4ATAC16P
    nsv3888812copy number variation1nstd102humanPathogenic GRCh38 chr12: 776,558-798,335 , GRCh37 chr12: 885,724-907,501 WNK1, RNU4ATAC16P
    nsv7095868copy number variation1nstd102humanPathogenic GRCh37 chr2: 167,083,057-167,099,186 , GRCh38.p12 chr2: 166,226,547-166,242,676 SCN9A, SCN1A-AS1
    nsv5673294copy number variation1nstd102humanPathogenic GRCh37 chr2: 167,055,172-167,060,984 , GRCh38.p12 chr2: 166,198,662-166,204,474 SCN9A, SCN1A-AS1
    nsv7095866copy number variation1nstd102humanPathogenic GRCh37 chr2: 167,055,182-167,056,394 , GRCh38.p12 chr2: 166,198,672-166,199,884 SCN1A-AS1, SCN9A
    nsv7096381copy number variation1nstd102humanLikely pathogenic GRCh37 chr2: 167,119,087-167,129,240 , GRCh38.p12 chr2: 166,262,577-166,272,730 SCN9A, SCN1A-AS1
    nsv4578667copy number variation1nstd102humanUncertain significance GRCh37 chr12: 862,732-1,017,641 , GRCh38.p12 chr12: 753,566-908,475 WNK1, RNU4ATAC16P
    nsv3885508copy number variation1nstd102humanUncertain significance GRCh37 chr2: 167,051,695-167,060,974 , GRCh38 chr2: 166,195,185-166,204,464 SCN9A, SCN1A-AS1
    nsv6311619copy number variation1nstd102humanUncertain significance GRCh37 chr2: 167,083,067-167,089,982 , GRCh38.p12 chr2: 166,226,557-166,233,472 SCN9A, SCN1A-AS1
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