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Items: 1 to 20 of 162

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099262copy number variation1nstd231human GRCh38.p12 chr1: 211,826,028-221,140,287 , GRCh37 chr1: 211,999,370-221,313,629 ATF3, CENPF, 114 more genes
    nsv7095503copy number variation1nstd102humanPathogenic GRCh37 chr1: 213,031,795-213,037,231 , GRCh38.p12 chr1: 212,858,453-212,863,889 FLVCR1-DT, FLVCR1
    nsv6671672copy number variation1nstd229human GRCh38 chr1: 212,832,753-213,257,197 , GRCh37.p13 chr1: 213,006,095-213,430,540 RPS28P2, RPS6KC1, 5 more genes
    nsv6638068copy number variation1nstd102humanassociation GRCh38 chr1: 208,430,918-228,938,006 , GRCh37.p13 chr1: 208,604,263-229,073,753 AURKAP1, TLR5, 372 more genes
    nsv6636965copy number variation1nstd102humanPathogenic GRCh37 chr1: 181,453,460-213,107,248 , GRCh38.p12 chr1: 181,484,324-212,933,906 PRELP, SYT14, 527 more genes
    nsv6634372copy number variation1nstd102humanPathogenic GRCh37 chr1: 197,867,914-249,224,684 , GRCh38.p12 chr1: 197,898,784-248,930,485 LOC105373279, YBX1P9, 1036 more genes
    nsv6626160copy number variation1nstd224human GRCh37 chr1: 213,029,879-213,130,756 , GRCh38.p12 chr1: 212,856,537-212,957,414 FLVCR1-DT, VASH2, 1 more genes
    nsv6626159copy number variation1nstd224human GRCh37 chr1: 213,005,012-213,046,088 , GRCh38.p12 chr1: 212,831,670-212,872,746 RPS28P2, FLVCR1, 2 more genes
    nsv6626158copy number variation3nstd224human GRCh37 chr1: 213,005,012-213,037,624 , GRCh38.p12 chr1: 212,831,670-212,864,282 FLVCR1-DT, FLVCR1, 2 more genes
    nsv6626157copy number variation5nstd224human GRCh37 chr1: 213,005,012-213,031,158 , GRCh38.p12 chr1: 212,831,670-212,857,816 SPATA45, RPS28P2, 2 more genes
    nsv6625968copy number variation1nstd224human GRCh37 chr1: 213,006,397-213,031,158 , GRCh38.p12 chr1: 212,833,055-212,857,816 FLVCR1, SPATA45, 2 more genes
    nsv6625960copy number variation1nstd224human GRCh37 chr1: 213,005,012-213,038,375 , GRCh38.p12 chr1: 212,831,670-212,865,033 FLVCR1-DT, FLVCR1, 2 more genes
    nsv6329396copy number variation1nstd223human GRCh38 chr1: 212,832,753-213,257,197 , GRCh37.p13 chr1: 213,006,095-213,430,540 FLVCR1, SPATA45, 5 more genes
    nsv6325553copy number variation1nstd223human GRCh38 chr1: 209,453,567-212,914,449 , GRCh37.p13 chr1: 209,626,912-213,087,791 ST13P19, RPS5P4, 74 more genes
    nsv6319488copy number variation1nstd223human GRCh38 chr1: 212,854,114-212,855,842 , GRCh37.p13 chr1: 213,027,456-213,029,184 FLVCR1-DT, RPS28P2
    nsv6291634copy number variation1nstd102humanUncertain significance GRCh38 chr1: 212,337,801-213,362,035 , GRCh37.p13 chr1: 212,511,143-213,535,378 ANGEL2, ATF3, 21 more genes
    nsv6290417copy number variation1nstd102humanUncertain significance GRCh37 chr1: 212,846,338-213,356,017 , GRCh38.p12 chr1: 212,672,996-213,182,674 NSL1, RPS6KC1, 9 more genes
    nsv6133848copy number variation1nstd213human GRCh37 chr1: 212,280,000-213,040,001 , GRCh38.p12 chr1: 212,106,658-212,866,659 NENF, GARIN4, 20 more genes
    nsv6133753copy number variation1nstd213human GRCh37 chr1: 210,410,000-214,880,001 , GRCh38.p12 chr1: 210,236,655-214,706,658 NEK2, PPP2R5A, 73 more genes
    nsv6133630copy number variation2nstd213human GRCh37 chr1: 206,490,000-223,720,001 , GRCh38.p12 chr1: 206,316,655-223,546,636 ATP5MC2P1, CENPF, 269 more genes
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