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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
    nsv6677134copy number variation1nstd229human GRCh38 chr1: 222,771,761-222,772,269 , GRCh37.p13 chr1: 222,945,103-222,945,611 FAM177B, LOC105372984
    nsv6675007copy number variation1nstd229human GRCh38 chr1: 222,711,079-223,231,899 , GRCh37.p13 chr1: 222,884,421-223,405,241 LOC102724046, FAM177B, 8 more genes
    nsv6674423copy number variation1nstd229human GRCh38 chr1: 222,731,728-222,748,497 , GRCh37.p13 chr1: 222,905,070-222,921,839 FAM177B, BROX
    nsv6672905copy number variation1nstd229human GRCh38 chr1: 222,763,601-222,766,000 , GRCh37.p13 chr1: 222,936,943-222,939,342 LOC105372984, FAM177B
    nsv6669861copy number variation1nstd229human GRCh38 chr1: 222,738,447-222,744,241 , GRCh37.p13 chr1: 222,911,789-222,917,583 FAM177B
    nsv6665559copy number variation1nstd229human GRCh38 chr1: 222,743,966-222,760,106 , GRCh37.p13 chr1: 222,917,308-222,933,448 LOC105372984, FAM177B
    nsv6661206copy number variation1nstd229human GRCh38 chr1: 222,753,701-222,755,700 , GRCh37.p13 chr1: 222,927,043-222,929,042 FAM177B, LOC105372984
    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
    nsv6335189copy number variation1nstd223human GRCh38 chr1: 222,743,961-222,760,100 , GRCh37.p13 chr1: 222,917,303-222,933,442 LOC105372984, FAM177B
    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
    nsv6322949copy number variation1nstd223human GRCh38 chr1: 222,771,759-222,772,266 , GRCh37.p13 chr1: 222,945,101-222,945,608 LOC105372984, FAM177B
    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
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