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Items: 1 to 20 of 155

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7099264copy number variation1nstd231human GRCh38.p12 chr1: 222,151,895-226,849,338 , GRCh37 chr1: 222,325,237-227,037,039 PARP1, CAPN2, 99 more genes
    nsv6658986copy number variation1nstd229human GRCh38 chr1: 222,438,201-222,485,800 , GRCh37.p13 chr1: 222,611,543-222,659,142 TRT-TGT2-1, LOC105372956, 2 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
    nsv6636736copy number variation1nstd102humanUncertain significance GRCh37 chr1: 221,325,488-225,804,228 , GRCh38.p12 chr1: 221,152,146-225,616,526 BROX, LINC02765, 77 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
    nsv6540195inversion1nstd223human GRCh38 chr1: 216,397,966-226,054,144 , GRCh37.p13 chr1: 216,571,308-226,241,845 LOC105373046, CNIH3-AS1, 154 more genes
    nsv6324615copy number variation1nstd223human GRCh38 chr1: 221,964,560-227,275,239 , GRCh37.p13 chr1: 222,137,902-227,462,940 LEFTY2, HHIPL2, 109 more genes
    nsv6313867copy number variation1nstd102humanUncertain significance GRCh37 chr1: 222,153,928-223,209,242 , GRCh38.p12 chr1: 221,980,586-223,035,900 MIA3, TAF1A-AS1, 18 more genes
    nsv6313779copy number variation1nstd102humanPathogenic GRCh37 chr1: 221,303,919-227,461,343 , GRCh38.p12 chr1: 221,130,577-227,273,642 ENAH, HHIPL2, 119 more genes
    nsv6290569copy number variation1nstd102humanPathogenic GRCh37 chr1: 215,199,578-223,035,427 , GRCh38.p12 chr1: 215,026,235-222,862,085 SPATA17, BROX, 97 more genes
    nsv6133860copy number variation1nstd213human GRCh37 chr1: 222,060,000-223,000,001 , GRCh38.p12 chr1: 221,886,658-222,826,659 MIA3, TAF1A-AS1, 18 more genes
    nsv6133857copy number variation1nstd213human GRCh37 chr1: 215,920,000-223,130,001 , GRCh38.p12 chr1: 215,746,658-222,956,659 BPNT1, HHIPL2, 95 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
    nsv6045536insertion1nstd212human GRCh38 chr1: 222,472,501-222,472,501 , GRCh37.p13 chr1: 222,645,843-222,645,843 LOC728417
    nsv6045359insertion1nstd212human GRCh38 chr1: 222,474,064-222,474,064 , GRCh37.p13 chr1: 222,647,406-222,647,406 LOC728417
    nsv6041908insertion1nstd212human GRCh38 chr1: 222,472,814-222,472,814 , GRCh37.p13 chr1: 222,646,156-222,646,156 LOC728417
    nsv5884342copy number variation1nstd209human GRCh38 chr1: 221,964,560-227,275,238 , GRCh37.p13 chr1: 222,137,902-227,462,939 , YBX1P9, 111 more genes
    nsv5616292insertion1nstd207human GRCh38 chr1: 222,474,050-222,474,050 , GRCh37.p13 chr1: 222,647,392-222,647,392 LOC728417
    nsv5582466copy number variation1nstd207human GRCh38 chr1: 222,476,200-222,476,609 , GRCh37.p13 chr1: 222,649,542-222,649,951 LOC728417
    nsv5571115copy number variation1nstd207human GRCh38 chr1: 222,475,250-222,475,699 , GRCh37.p13 chr1: 222,648,592-222,649,041 LOC728417
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