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Items: 1 to 20 of 231

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139933copy number variation1nstd232human GRCh37.p13 chr2: 172,414,924-172,414,986 , GRCh38.p12 chr2: 171,558,414-171,558,476 CYBRD1
    nsv7096586copy number variation1nstd102humanUncertain significance GRCh37 chr2: 171,675,102-174,232,392 , GRCh38.p12 chr2: 170,818,592-173,367,664 RNU6-182P, DCAF17, 36 more genes
    nsv7048425inversion1nstd229human GRCh38 chr2: 171,556,180-171,565,999 , GRCh37.p13 chr2: 172,412,690-172,422,509 CYBRD1
    nsv6681251copy number variation1nstd229human GRCh38 chr2: 171,539,735-171,551,918 , GRCh37.p13 chr2: 172,396,245-172,408,428 CYBRD1
    nsv6679064copy number variation1nstd229human GRCh38 chr2: 171,528,396-171,528,470 , GRCh37.p13 chr2: 172,384,906-172,384,980 CYBRD1
    nsv6553033inversion1nstd223human GRCh38 chr2: 171,528,216-171,529,273 , GRCh37.p13 chr2: 172,384,726-172,385,783 CYBRD1
    nsv6552834inversion1nstd223human GRCh38 chr2: 171,544,857-171,545,414 , GRCh37.p13 chr2: 172,401,367-172,401,924 CYBRD1
    nsv6550352inversion1nstd223human GRCh38 chr2: 171,538,217-171,538,790 , GRCh37.p13 chr2: 172,394,727-172,395,300 CYBRD1
    nsv6539679inversion1nstd223human GRCh38 chr2: 171,539,368-171,539,753 , GRCh37.p13 chr2: 172,395,878-172,396,263 CYBRD1
    nsv6354047copy number variation1nstd223human GRCh38 chr2: 171,541,923-171,542,080 , GRCh37.p13 chr2: 172,398,433-172,398,590 CYBRD1
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6315160copy number variation1nstd102humanPathogenic GRCh37 chr2: 160,347,642-174,075,851 , GRCh38.p12 chr2: 159,491,131-173,211,123 EIF3EP3, FAP, 158 more genes
    nsv6315016copy number variation1nstd102humanPathogenic GRCh37 chr2: 171,524,396-178,694,337 , GRCh38.p12 chr2: 170,667,886-177,829,610 LOC105373746, HAGLROS, 136 more genes
    nsv6164500copy number variation1nstd214human GRCh38 chr2: 171,558,319-171,558,384 , GRCh37.p13 chr2: 172,414,829-172,414,894 CYBRD1
    nsv6159029copy number variation1nstd214human GRCh38 chr2: 171,558,401-171,558,476 , GRCh37.p13 chr2: 172,414,911-172,414,986 CYBRD1
    nsv6149000copy number variation1nstd214human GRCh38 chr2: 171,558,414-171,558,476 , GRCh37.p13 chr2: 172,414,924-172,414,986 CYBRD1
    nsv6134500copy number variation1nstd213human GRCh37 chr2: 149,790,000-179,310,001 , GRCh38.p12 chr2: 148,934,069-178,445,274 , ACVR1, 394 more genes
    nsv6054319insertion1nstd212human GRCh38 chr2: 171,535,577-171,535,577 , GRCh37.p13 chr2: 172,392,087-172,392,087 CYBRD1
    nsv6053158insertion1nstd212human GRCh38 chr2: 171,558,477-171,558,477 , GRCh37.p13 chr2: 172,414,987-172,414,987 CYBRD1
    nsv6051088insertion1nstd212human GRCh38 chr2: 171,558,379-171,558,379 , GRCh37.p13 chr2: 172,414,889-172,414,889 CYBRD1
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