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Items: 1 to 20 of 274

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7057471inversion1nstd229human GRCh38 chr2: 233,346,794-233,351,583 , GRCh37.p13 chr2: 234,255,440-234,260,229 SAG
    nsv7049654inversion1nstd229human GRCh38 chr2: 233,236,665-233,574,597 , GRCh37.p13 chr2: 234,145,311-234,483,243 DGKD, SAG, 5 more genes
    nsv7046425inversion1nstd229human GRCh38 chr2: 233,334,328-233,334,369 , GRCh37.p13 chr2: 234,242,974-234,243,015 SAG
    nsv7041487inversion1nstd229human GRCh38 chr2: 233,277,178-233,725,509 , GRCh37.p13 chr2: 234,185,824-234,634,155 SCARNA6, UGT1A5, 16 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
    nsv6694251copy number variation1nstd229human GRCh38 chr2: 233,277,028-233,460,169 , GRCh37.p13 chr2: 234,185,674-234,368,815 ATG16L1, SCARNA6, 2 more genes
    nsv6693319copy number variation1nstd229human GRCh38 chr2: 233,311,901-233,314,000 , GRCh37.p13 chr2: 234,220,547-234,222,646 SAG
    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
    nsv6688296copy number variation1nstd229human GRCh38 chr2: 233,328,664-233,328,977 , GRCh37.p13 chr2: 234,237,310-234,237,623 SAG
    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
    nsv6683796copy number variation1nstd229human GRCh38 chr2: 233,304,103-233,306,534 , GRCh37.p13 chr2: 234,212,749-234,215,180 SAG
    nsv6683179copy number variation1nstd229human GRCh38 chr2: 233,310,905-233,310,962 , GRCh37.p13 chr2: 234,219,551-234,219,608 SAG
    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
    nsv6336751copy number variation1nstd223human GRCh38 chr2: 233,310,767-233,317,122 , GRCh37.p13 chr2: 234,219,413-234,225,768 SAG
    nsv6335929copy number variation1nstd223human GRCh38 chr2: 233,333,456-233,337,347 , GRCh37.p13 chr2: 234,242,102-234,245,993 SAG
    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
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