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Items: 1 to 20 of 110

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7049654inversion1nstd229human GRCh38 chr2: 233,236,665-233,574,597 , GRCh37.p13 chr2: 234,145,311-234,483,243 DGKD, SAG, 5 more genes
    nsv6695695copy number variation1nstd229human GRCh38 chr2: 233,232,967-233,543,299 , GRCh37.p13 chr2: 234,141,613-234,451,945 USP40, SCARNA5, 4 more genes
    nsv6695110copy number variation1nstd229human GRCh38 chr2: 233,112,247-233,292,742 , GRCh37.p13 chr2: 233,976,957-234,201,388 SCARNA6, ATG16L1, 3 more genes
    nsv6689588copy number variation1nstd229human GRCh38 chr2: 233,275,591-233,335,266 , GRCh37.p13 chr2: 234,184,237-234,243,912 SCARNA5, ATG16L1, 2 more genes
    nsv6689043copy number variation1nstd229human GRCh38 chr2: 233,061,229-233,370,687 , GRCh37.p13 chr2: 233,925,939-234,279,333 INPP5D, SAG, 5 more genes
    nsv6686173copy number variation1nstd229human GRCh38 chr2: 233,271,953-233,322,386 , GRCh37.p13 chr2: 234,180,599-234,231,032 ATG16L1, SAG, 2 more genes
    nsv6679072copy number variation1nstd229human GRCh38 chr2: 233,093,901-233,643,200 , GRCh37.p13 chr2: 233,958,611-234,551,846 DGKD, INPP5D, 12 more genes
    nsv6636912copy number variation1nstd102humanUncertain significance GRCh37 chr2: 233,642,145-237,654,870 , GRCh38.p12 chr2: 232,777,435-236,746,227 UGT1A, SH3BP4, 70 more genes
    nsv6628068copy number variation1nstd224human GRCh37 chr2: 234,178,662-234,255,047 , GRCh38.p12 chr2: 233,270,016-233,346,401 , GRCh38.p12 chr2|NW_011332690.1: 215,354-291,739 SAG, ATG16L1, 2 more genes
    nsv6338498copy number variation1nstd223human GRCh38 chr2: 233,275,591-233,335,263 , GRCh37.p13 chr2: 234,184,237-234,243,909 ATG16L1, SAG, 2 more genes
    nsv6315436copy number variation1nstd102humanPathogenic GRCh37 chr2: 233,227,837-242,783,384 , GRCh38.p12 chr2: 232,363,127-241,841,232 LOC105373929, LOC105373932, 204 more genes
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6313683copy number variation1nstd102humanPathogenic GRCh37 chr2: 228,807,574-235,475,892 , GRCh38.p12 chr2: 227,942,858-234,567,248 RNU7-9P, SCARNA5, 143 more genes
    nsv6313668copy number variation1nstd102humanPathogenic GRCh37 chr2: 219,606,537-239,217,703 , GRCh38.p12 chr2: 218,741,814-238,309,062 LOC105373947, RN7SL764P, 357 more genes
    nsv6311650copy number variation2nstd102humanUncertain significance GRCh37 chr2: 231,033,840-234,978,657 , GRCh38.p12 chr2: 230,169,124-234,070,013 SP110, LINC00471, 112 more genes
    nsv6311386copy number variation1nstd102humanUncertain significance GRCh37 chr2: 233,164,730-234,250,992 , GRCh38.p12 chr2: 232,300,020-233,342,346 DIS3L2P1, TIGD1, 31 more genes
    nsv5216097copy number variation1nstd204human GRCh38.p13 chr2: 232,998,601-233,432,200 , GRCh37.p13 chr2: 233,863,311-234,340,846 SAG, ATG16L1, 8 more genes
    nsv5214863copy number variation1nstd204human GRCh38.p13 chr2: 233,275,685-233,277,684 , GRCh37.p13 chr2: 234,184,331-234,186,330 ATG16L1, SCARNA5
    nsv5211394copy number variation1nstd204human GRCh38.p13 chr2: 233,225,406-233,274,034 , GRCh37.p13 chr2: 234,134,052-234,182,680 ATG16L1, SCARNA5
    nsv5210089copy number variation1nstd204human GRCh38.p13 chr2: 233,247,201-233,274,534 , GRCh37.p13 chr2: 234,155,847-234,183,180 SCARNA5, ATG16L1
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