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Items: 1 to 20 of 229

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    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
    nsv6697297copy number variation1nstd229human GRCh38 chr2: 171,478,496-171,489,243 , GRCh37.p13 chr2: 172,335,006-172,345,753 DCAF17
    nsv6685006copy number variation1nstd229human GRCh38 chr2: 171,386,522-171,487,526 , GRCh37.p13 chr2: 172,243,032-172,344,036 DCAF17, METTL8
    nsv6679153copy number variation1nstd229human GRCh38 chr2: 171,365,156-171,441,495 , GRCh37.p13 chr2: 172,221,666-172,298,005 METTL8, DCAF17, 1 more genes
    nsv6551721inversion1nstd223human GRCh38 chr2: 171,459,999-171,460,681 , GRCh37.p13 chr2: 172,316,509-172,317,191 DCAF17
    nsv6549732inversion1nstd223human GRCh38 chr2: 171,446,263-171,447,665 , GRCh37.p13 chr2: 172,302,773-172,304,175 DCAF17
    nsv6545080inversion1nstd223human GRCh38 chr2: 171,489,650-171,491,042 , GRCh37.p13 chr2: 172,346,160-172,347,552 DAP3P2, DCAF17
    nsv6542957inversion1nstd223human GRCh38 chr2: 171,464,943-171,465,651 , GRCh37.p13 chr2: 172,321,453-172,322,161 DCAF17
    nsv6541023inversion1nstd223human GRCh38 chr2: 171,454,163-171,454,421 , GRCh37.p13 chr2: 172,310,673-172,310,931 DCAF17
    nsv6539134inversion1nstd223human GRCh38 chr2: 171,471,723-171,472,342 , GRCh37.p13 chr2: 172,328,233-172,328,852 DCAF17
    nsv6350956copy number variation1nstd223human GRCh38 chr2: 171,431,801-171,439,000 , GRCh37.p13 chr2: 172,288,311-172,295,510 METTL8, DCAF17
    nsv6350754copy number variation1nstd223human GRCh38 chr2: 171,461,601-171,462,600 , GRCh37.p13 chr2: 172,318,111-172,319,110 DCAF17
    nsv6348287copy number variation1nstd223human GRCh38 chr2: 171,460,228-171,461,323 , GRCh37.p13 chr2: 172,316,738-172,317,833 DCAF17
    nsv6340078copy number variation1nstd223human GRCh38 chr2: 171,386,522-171,487,524 , GRCh37.p13 chr2: 172,243,032-172,344,034 DCAF17, METTL8
    nsv6338305copy number variation1nstd223human GRCh38 chr2: 171,435,001-171,439,800 , GRCh37.p13 chr2: 172,291,511-172,296,310 DCAF17, METTL8
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 more genes
    nsv6315312copy number variation1nstd102humanUncertain significance GRCh37 chr2: 172,290,760-172,341,563 , GRCh38.p12 chr2: 171,434,250-171,485,053 DCAF17, METTL8
    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
    nsv6134500copy number variation1nstd213human GRCh37 chr2: 149,790,000-179,310,001 , GRCh38.p12 chr2: 148,934,069-178,445,274 , ACVR1, 394 more genes
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