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Items: 1 to 20 of 253

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7055249inversion1nstd229human GRCh38 chr5: 44,753,059-44,763,310 , GRCh37.p13 chr5: 44,753,161-44,763,412 MRPS30-DT
    nsv7041959inversion1nstd229human GRCh38 chr5: 44,756,724-44,763,138 , GRCh37.p13 chr5: 44,756,826-44,763,240 MRPS30-DT
    nsv7040713inversion1nstd229human GRCh38 chr5: 44,325,839-45,047,347 , GRCh37.p13 chr5: 44,325,941-45,047,449 MRPS30, FGF10, 4 more genes
    nsv6775784copy number variation1nstd229human GRCh38 chr5: 44,794,894-44,795,468 , GRCh37.p13 chr5: 44,794,996-44,795,570 MRPS30-DT
    nsv6774344copy number variation1nstd229human GRCh38 chr5: 44,772,173-44,780,623 , GRCh37.p13 chr5: 44,772,275-44,780,725 MRPS30-DT
    nsv6771396copy number variation1nstd229human GRCh38 chr5: 44,807,901-44,809,500 , GRCh37.p13 chr5: 44,808,003-44,809,602 MRPS30-DT, MRPS30
    nsv6770703copy number variation1nstd229human GRCh38 chr5: 44,796,785-44,801,682 , GRCh37.p13 chr5: 44,796,887-44,801,784 MRPS30-DT
    nsv6767540copy number variation1nstd229human GRCh38 chr5: 44,787,929-44,788,009 , GRCh37.p13 chr5: 44,788,031-44,788,111 MRPS30-DT
    nsv6764263copy number variation1nstd229human GRCh38 chr5: 44,696,803-44,807,074 , GRCh37.p13 chr5: 44,696,905-44,807,176 MRPS30, RN7SL383P, 1 more genes
    nsv6636973copy number variation1nstd102humanPathogenic GRCh37 chr5: 29,348,753-46,389,339 , GRCh38.p12 chr5: 29,348,646-46,389,237 SUB1, LOC105374740, 210 more genes
    nsv6630408copy number variation1nstd224human GRCh37 chr5: 44,727,706-45,354,799 , GRCh38.p12 chr5: 44,727,604-45,354,697 MRPS30-DT, MRPS30, 1 more genes
    nsv6392191copy number variation1nstd223human GRCh38 chr5: 44,774,538-44,775,129 , GRCh37.p13 chr5: 44,774,640-44,775,231 MRPS30-DT
    nsv6391574copy number variation1nstd223human GRCh38 chr5: 44,794,894-44,795,468 , GRCh37.p13 chr5: 44,794,996-44,795,570 MRPS30-DT
    nsv6391517copy number variation1nstd223human GRCh38 chr5: 44,749,164-44,749,550 , GRCh37.p13 chr5: 44,749,266-44,749,652 MRPS30-DT
    nsv6386050copy number variation1nstd223human GRCh38 chr5: 44,743,548-44,744,098 , GRCh37.p13 chr5: 44,743,650-44,744,200 MRPS30-DT
    nsv6377973copy number variation1nstd223human GRCh38 chr5: 44,689,254-45,062,105 , GRCh37.p13 chr5: 44,689,356-45,062,207 RN7SL383P, MRPS30-DT, 1 more genes
    nsv6377683copy number variation1nstd223human GRCh38 chr5: 44,744,057-44,744,589 , GRCh37.p13 chr5: 44,744,159-44,744,691 MRPS30-DT
    nsv6315368copy number variation1nstd102humanPathogenic GRCh37 chr5: 36,053,583-46,389,339 , GRCh38.p12 chr5: 36,053,481-46,389,237 C7, RIMOC1, 128 more genes
    nsv6315286copy number variation1nstd102humanUncertain significance GRCh38 chr5: 44,375,961-44,815,730 , GRCh37.p13 chr5: 44,376,063-44,815,832 FGF10-AS1, LINC02224, 4 more genes
    nsv6313864copy number variation1nstd102humanPathogenic GRCh37 chr5: 26,382,110-46,389,339 , GRCh38.p12 chr5: 26,382,001-46,389,237 LOC107986346, RNU6-760P, 227 more genes
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