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Items: 1 to 20 of 442

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7093212copy number variation1nstd102humanUncertain significance GRCh38 chr2: 157,737,327-157,737,616 , GRCh37 chr2: 158,593,839-158,594,128 ACVR1
    nsv7056410inversion1nstd229human GRCh38 chr2: 155,671,571-160,808,437 , GRCh37.p13 chr2: 156,528,083-161,664,948 LOC105373714, PKP4-AS1, 64 more genes
    nsv7048490inversion1nstd229human GRCh38 chr2: 156,054,444-158,055,095 , GRCh37.p13 chr2: 156,910,956-158,911,607 CYTIP, LINC01876, 23 more genes
    nsv7039204inversion1nstd229human GRCh38 chr2: 157,849,470-157,849,572 , GRCh37.p13 chr2: 158,705,982-158,706,084 ACVR1
    nsv7038090inversion1nstd229human GRCh38 chr2: 152,079,952-160,943,714 , GRCh37.p13 chr2: 152,936,466-161,800,225 , ITGB6, 105 more genes
    nsv6697351copy number variation1nstd229human GRCh38 chr2: 157,835,146-158,258,896 , GRCh37.p13 chr2: 158,691,658-159,115,408 ACVR1, UPP2, 7 more genes
    nsv6696577copy number variation1nstd229human GRCh38 chr2: 157,829,827-157,829,928 , GRCh37.p13 chr2: 158,686,339-158,686,440 ACVR1
    nsv6696229copy number variation1nstd229human GRCh38 chr2: 157,841,622-157,845,584 , GRCh37.p13 chr2: 158,698,134-158,702,096 ACVR1
    nsv6695398copy number variation1nstd229human GRCh38 chr2: 157,862,588-157,862,884 , GRCh37.p13 chr2: 158,719,100-158,719,396 ACVR1
    nsv6690828copy number variation1nstd229human GRCh38 chr2: 157,854,492-157,863,424 , GRCh37.p13 chr2: 158,711,004-158,719,936 ACVR1
    nsv6689275copy number variation1nstd229human GRCh38 chr2: 157,762,166-157,762,685 , GRCh37.p13 chr2: 158,618,678-158,619,197 ACVR1
    nsv6686303copy number variation1nstd229human GRCh38 chr2: 157,819,220-157,821,242 , GRCh37.p13 chr2: 158,675,732-158,677,754 ACVR1
    nsv6686257copy number variation1nstd229human GRCh38 chr2: 157,755,392-157,756,384 , GRCh37.p13 chr2: 158,611,904-158,612,896 ACVR1
    nsv6686221copy number variation1nstd229human GRCh38 chr2: 157,749,668-157,753,629 , GRCh37.p13 chr2: 158,606,180-158,610,141 ACVR1
    nsv6685979copy number variation1nstd229human GRCh38 chr2: 157,752,524-157,754,540 , GRCh37.p13 chr2: 158,609,036-158,611,052 ACVR1
    nsv6685698copy number variation1nstd229human GRCh38 chr2: 157,872,861-157,873,341 , GRCh37.p13 chr2: 158,729,373-158,729,853 ACVR1
    nsv6683078copy number variation1nstd229human GRCh38 chr2: 154,503,385-158,170,825 , GRCh37.p13 chr2: 155,359,897-159,027,337 HEBP2P1, RNU6-436P, 48 more genes
    nsv6680292copy number variation1nstd229human GRCh38 chr2: 157,841,284-157,841,446 , GRCh37.p13 chr2: 158,697,796-158,697,958 ACVR1
    nsv6679833copy number variation1nstd229human GRCh38 chr2: 157,230,726-158,497,988 , GRCh37.p13 chr2: 158,087,238-159,354,500 LOC105373714, ERMN, 17 more genes
    nsv6678233copy number variation1nstd229human GRCh38 chr2: 157,814,701-157,840,700 , GRCh37.p13 chr2: 158,671,213-158,697,212 ACVR1
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