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Items: 1 to 20 of 314

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7049124inversion1nstd229human GRCh38 chr2: 174,401,435-175,981,960 , GRCh37.p13 chr2: 175,266,163-176,846,688 LNPK, RNU7-44P, 19 more genes
    nsv7044100inversion1nstd229human GRCh38 chr2: 174,492,815-174,493,479 , GRCh37.p13 chr2: 175,357,543-175,358,207 GPR155
    nsv6692172copy number variation1nstd229human GRCh38 chr2: 174,464,641-174,483,387 , GRCh37.p13 chr2: 175,329,369-175,348,115 GPR155
    nsv6691749copy number variation1nstd229human GRCh38 chr2: 174,489,064-174,513,590 , GRCh37.p13 chr2: 175,353,792-175,378,318 RPA3P1, GPR155-DT, 1 more genes
    nsv6690461copy number variation1nstd229human GRCh38 chr2: 174,482,902-174,497,778 , GRCh37.p13 chr2: 175,347,630-175,362,506 GPR155, GPR155-DT
    nsv6690248copy number variation1nstd229human GRCh38 chr2: 174,490,400-174,498,999 , GRCh37.p13 chr2: 175,355,128-175,363,727 GPR155
    nsv6689002copy number variation1nstd229human GRCh38 chr2: 174,435,916-174,438,901 , GRCh37.p13 chr2: 175,300,644-175,303,629 GPR155
    nsv6686569copy number variation1nstd229human GRCh38 chr2: 174,387,000-174,456,868 , GRCh37.p13 chr2: 175,251,728-175,321,596 CIR1, GPR155, 1 more genes
    nsv6685862copy number variation1nstd229human GRCh38 chr2: 174,403,084-174,465,728 , GRCh37.p13 chr2: 175,267,812-175,330,456 SCRN3, GPR155
    nsv6637115copy number variation1nstd102humanPathogenic GRCh37 chr2: 175,143,352-180,999,636 , GRCh38.p12 chr2: 174,278,624-180,134,909 RNU6-5P, LOC101927073, 107 more genes
    nsv6627283copy number variation1nstd224human GRCh37 chr2: 175,263,063-175,316,379 , GRCh38.p12 chr2: 174,398,335-174,451,651 GPR155, SCRN3
    nsv6553881inversion1nstd223human GRCh38 chr2: 174,494,082-174,495,021 , GRCh37.p13 chr2: 175,358,810-175,359,749 GPR155
    nsv6550891inversion1nstd223human GRCh38 chr2: 174,466,890-174,467,938 , GRCh37.p13 chr2: 175,331,618-175,332,666 GPR155
    nsv6545350inversion1nstd223human GRCh38 chr2: 174,437,839-174,438,242 , GRCh37.p13 chr2: 175,302,567-175,302,970 GPR155
    nsv6315390copy number variation1nstd102humanPathogenic GRCh37 chr2: 1-243,199,373 , GRCh38.p12 chr2: 10,001-242,157,305 LOC112268439, RNA5SP116, 3737 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
    nsv6291326copy number variation1nstd102humannot provided GRCh37 chr2: 174,631,045-177,365,790 , GRCh38.p12 chr2: 173,766,317-176,501,062 RNU6-5P, RPS15AP14, 56 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
    nsv6058429insertion1nstd212human GRCh38 chr2: 174,454,886-174,454,886 , GRCh37.p13 chr2: 175,319,614-175,319,614 GPR155
    nsv6051298insertion1nstd212human GRCh38 chr2: 174,458,291-174,458,291 , GRCh37.p13 chr2: 175,323,019-175,323,019 GPR155
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