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Items: 1 to 20 of 222

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv5355499translocation1nstd200human GRCh38 chr20: 9,175,252-9,175,252 , GRCh38 chr12: 7,711,424-7,711,424 , GRCh37.p13 chr20: 9,155,899-9,155,899 , GRCh37.p13 chr12: 7,864,020-7,864,020 PLCB4, DPPA3
    nsv5339354translocation1nstd200human GRCh37 chr12: 7,864,020-7,864,020 , GRCh37 chr20: 9,155,900-9,155,900 , GRCh38.p12 chr12: 7,711,424-7,711,424 , GRCh38.p12 chr20: 9,175,253-9,175,253 DPPA3, PLCB4
    nsv5323122inversion1nstd204human GRCh37.p13 chr12: 6,338,815-22,046,498 , GRCh38.p13 chr12: 6,229,649-21,893,564 , A2M, 414 more genes
    nsv5264468copy number variation1nstd204human GRCh38.p13 chr12: 7,619,401-7,984,600 , GRCh37.p13 chr12: 7,771,997-8,137,196 SLC2A3, CLEC4C, 9 more genes
    nsv5139423mobile element insertion1nstd203human GRCh38 chr12: 7,712,075-7,712,077 , GRCh37.p13 chr12: 7,864,671-7,864,673 DPPA3
    nsv5138120mobile element insertion1nstd203human GRCh38 chr12: 7,712,081-7,712,088 , GRCh37.p13 chr12: 7,864,677-7,864,684 DPPA3
    nsv5127963mobile element insertion1nstd203human GRCh38 chr12: 7,711,390-7,711,407 , GRCh37.p13 chr12: 7,863,986-7,864,003 DPPA3
    nsv5126497mobile element insertion1nstd203human GRCh38 chr12: 7,712,030-7,712,077 , GRCh37.p13 chr12: 7,864,626-7,864,673 DPPA3
    nsv5124814mobile element insertion1nstd203human GRCh38 chr12: 7,712,077-7,712,088 , GRCh37.p13 chr12: 7,864,673-7,864,684 DPPA3
    nsv5123873mobile element insertion1nstd203human GRCh38 chr12: 7,711,720-7,711,750 , GRCh37.p13 chr12: 7,864,316-7,864,346 DPPA3
    nsv5122046mobile element insertion1nstd203human GRCh38 chr12: 7,712,082-7,712,088 , GRCh37.p13 chr12: 7,864,678-7,864,684 DPPA3
    nsv5120100mobile element insertion1nstd203human GRCh38 chr12: 7,712,076-7,712,088 , GRCh37.p13 chr12: 7,864,672-7,864,684 DPPA3
    nsv5029743inversion1nstd200human GRCh38 chr12: 7,297,013-15,308,349 , GRCh37.p13 chr12: 7,449,609-15,461,283 , MIR1244-4, 259 more genes
    nsv4972074copy number variation1nstd200human GRCh38 chr12: 7,709,601-7,712,522 , GRCh37.p13 chr12: 7,862,197-7,865,118 DPPA3
    nsv4972073copy number variation1nstd200human GRCh38 chr12: 7,709,841-7,709,935 , GRCh37.p13 chr12: 7,862,437-7,862,531 DPPA3
    nsv4882300inversion1nstd200human GRCh37 chr12: 6,338,820-22,046,498 , GRCh38.p12 chr12: 6,229,654-21,893,564 , LOC105369686, 414 more genes
    nsv4833406copy number variation1nstd200human GRCh37 chr12: 7,862,257-7,865,090 , GRCh38.p12 chr12: 7,709,661-7,712,494 DPPA3
    nsv4729082copy number variation1nstd102humanLikely benign GRCh37 chr12: 7,755,907-8,436,318 , GRCh38.p12 chr12: 7,603,311-8,283,722 NANOGP1, RPS20P29, 29 more genes
    nsv4682301copy number variation1nstd102humanUncertain significance GRCh37 chr12: 6,945,914-8,248,706 , GRCh38.p12 chr12: 6,836,750-8,096,110 SPSB2, LOC100131676, 57 more genes
    nsv4681373copy number variation1nstd102humanUncertain significance GRCh37 chr12: 7,842,454-8,248,706 , GRCh38.p12 chr12: 7,689,858-8,096,110 NANOGP1, LOC100462988, 14 more genes
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