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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3887315copy number variation1nstd102humanBenign GRCh37 chr1: 239,832,680-239,867,143 , GRCh38.p12 chr1: 239,669,380-239,703,843 CHRM3
    nsv4674264copy number variation1nstd102humanUncertain significance GRCh37 chr1: 239,823,151-239,862,101 , GRCh38.p12 chr1: 239,659,851-239,698,801 CHRM3
    nsv7095603copy number variation1nstd102humanUncertain significance GRCh37 chr1: 240,070,603-240,072,524 , GRCh38.p12 chr1: 239,907,303-239,909,224 CHRM3
    nsv3873245copy number variation1nstd102humanBenign GRCh37 chr1: 239,774,393-239,828,164 , GRCh38.p12 chr1: 239,611,093-239,664,864 CHRM3, LOC105373225
    nsv3873855copy number variation1nstd102humanBenign GRCh37 chr1: 239,774,393-239,813,953 , GRCh38.p12 chr1: 239,611,093-239,650,653 CHRM3, LOC105373225
    nsv3881335copy number variation1nstd102humanBenign GRCh37 chr1: 239,350,728-239,574,661 , GRCh38.p12 chr1: 239,187,428-239,411,361 CHRM3, LOC105373223
    nsv6637059copy number variation1nstd102humanUncertain significance GRCh37 chr1: 239,786,186-239,808,882 , GRCh38.p12 chr1: 239,622,886-239,645,582 CHRM3, LOC105373225
    nsv4728348copy number variation1nstd102humanUncertain significance GRCh37 chr1: 239,330,625-239,581,669 , GRCh38.p12 chr1: 239,167,325-239,418,369 CHRM3, LOC105373223
    nsv3885149copy number variation1nstd102humannot provided GRCh38 chr1: 239,551,474-239,621,865 , GRCh37 chr1: 239,714,774-239,785,165 CHRM3, LOC105373225
    esv3648587copy number variation1estd216humannot provided GRCh38.p12 chr1: 239,551,474-239,621,865 , GRCh37 chr1: 239,714,774-239,785,165 CHRM3, LOC105373225
    nsv3900131copy number variation1nstd102humanUncertain significance GRCh38 chr1: 239,777,071-240,028,234 , NCBI36 chr1: 238,006,994-238,258,157 , GRCh37 chr1: 239,940,371-240,191,534 CHRM3, LOC105373224, 3 more genes
    nsv4728287copy number variation1nstd102humanUncertain significance GRCh37 chr1: 239,367,007-239,974,659 , GRCh38.p12 chr1: 239,203,707-239,811,359 CHRM3, CHRM3-AS2, 2 more genes
    nsv4452161copy number variation1nstd102humanUncertain significance GRCh37 chr1: 239,601,103-239,965,763 , GRCh38.p12 chr1: 239,437,803-239,802,463 CHRM3, CHRM3-AS2, 1 more genes
    nsv3888727copy number variation1nstd102humanUncertain significance GRCh37 chr1: 239,678,218-239,969,806 , GRCh38.p12 chr1: 239,514,918-239,806,506 CHRM3, CHRM3-AS2, 1 more genes
    nsv6634337copy number variation1nstd102humanPathogenic GRCh37 chr1: 233,012,994-249,206,918 , GRCh38.p12 chr1: 232,877,248-248,912,719 CHRM3, OR2M4, 316 more genes
    nsv3904200copy number variation1nstd102humanPathogenic GRCh38 chr1: 230,106,271-243,677,283 , NCBI36 chr1: 228,308,641-241,907,208 , GRCh37 chr1: 230,242,018-243,840,585 CHRM3, MIR3123, 221 more genes
    nsv7148175copy number variation1nstd102humanPathogenic GRCh38 chr1: 230,178,121-243,646,135 , GRCh37.p13 chr1: 230,313,867-243,809,437 CHRM3, AGT, 221 more genes
    nsv3876145copy number variation1nstd102humanPathogenic GRCh37 chr1: 235,797,384-249,224,684 , GRCh38.p12 chr1: 235,634,084-248,930,485 CHRM3, OR11L1, 257 more genes
    nsv3893126copy number variation1nstd102humanPathogenic GRCh37 chr1: 236,719,382-249,212,668 , GRCh38 chr1: 236,556,082-248,918,469 , NCBI36 chr1: 234,786,005-247,179,291 CHRM3, RNU6-1205P, 239 more genes
    nsv7148158copy number variation1nstd102humanPathogenic GRCh38 chr1: 235,215,476-247,005,888 , GRCh37.p13 chr1: 235,378,791-247,169,190 CHRM3, RNU6-747P, 172 more genes
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