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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3131368copy number variation1nstd151human GRCh37 (hg19) chr4: 90,647,776-90,874,574 , GRCh38 (hg38) chr4: 89,726,625-89,953,423 MMRN1, SNCA-AS1, 1 more genes
    nsv3125980copy number variation1nstd151human GRCh37 (hg19) chr4: 83,891,477-90,874,574 , GRCh38 (hg38) chr4: 82,970,324-89,953,423 AFF1-AS1, MIR4451, 48 more genes
    nsv3110061copy number variation1nstd37humanLikely pathogenic GRCh37 (hg19) chr4: 89,891,197-98,235,479 , GRCh38 (hg38) chr4: 88,970,046-97,314,328 , NCBI36 (hg18) chr4: 90,110,220-98,454,502 BMPR1B-AS1, RNA5SP164, 19 more genes
    nsv3110060copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr4: 85,469,728-94,794,648 , GRCh37 (hg19) chr4: 85,250,704-94,575,625 , GRCh38 (hg38) chr4: 84,329,551-93,654,474 AFF1-AS1, MIR4451, 43 more genes
    esv4010685copy number variation1estd233human GRCh37 (hg19) chr4: 80,275,000-126,342,000 , GRCh38 (hg38) chr4: 79,353,846-125,420,845 SNHG8, MIR297, 244 more genes
    nsv3084286mobile element insertion1nstd144human GRCh37 (hg19) chr4: 90,706,799-90,706,799 , GRCh38 (hg38) chr4: 89,785,648-89,785,648 SNCA
    nsv3046289insertion1nstd140human GRCh38 (hg38) chr4: 89,821,303-89,821,304 , GRCh37 (hg19) chr4: 90,742,454-90,742,455 SNCA
    nsv2775308copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr4: 88,484,512-94,794,609 , GRCh37 (hg19) chr4: 88,265,488-94,575,586 , GRCh38 (hg38) chr4: 87,344,336-93,654,435 RNU6-33P, PYURF, 27 more genes
    nsv2773758copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr4: 85,805,268-103,678,797 , GRCh38 (hg38) chr4: 84,884,115-102,757,640 , NCBI36 (hg18) chr4: 86,024,292-103,897,840 MIR1255A, MIR3684, 86 more genes
    nsv2773339copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr4: 12,440-190,904,441 , GRCh38 (hg38) chr4: 12,440-189,983,286 , NCBI36 (hg18) chr4: 2,440-191,141,435 SNHG8, MIR943, 1039 more genes
    nsv2772086copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr4: 75,737,340-91,131,156 , GRCh38 (hg38) chr4: 74,812,130-90,210,005 , NCBI36 (hg18) chr4: 75,956,364-91,350,179 FAM47E, THAP9-AS1, 112 more genes
    nsv2771017copy number variation1nstd37humanPathogenic NCBI36 (hg18) chr4: 58,862,002-102,129,682 , GRCh37 (hg19) chr4: 59,167,245-101,910,659 , GRCh38 (hg38) chr4: 58,301,079-100,989,502 FAM47E, EPHA5-AS1, 240 more genes
    nsv2770921copy number variation1nstd37humanPathogenic GRCh37 (hg19) chr4: 85,839,771-93,071,150 , GRCh38 (hg38) chr4: 84,918,618-92,149,999 , NCBI36 (hg18) chr4: 86,058,795-93,290,173 AFF1-AS1, MIR4451, 39 more genes
    nsv2769375copy number variation2nstd37humanPathogenic GRCh37 (hg19) chr4: 68,346-190,957,473 , GRCh38 (hg38) chr4: 68,454-190,036,318 , NCBI36 (hg18) chr4: 58,346-191,194,467 SNHG8, MIR943, 1041 more genes
    esv3836091copy number variation197estd219human GRCh37 (hg19) chr4: 90,648,814-90,648,905 , GRCh38 (hg38) chr4: 89,727,663-89,727,754 SNCA
    esv3836092mobile element insertion9estd219human GRCh37 (hg19) chr4: 90,706,799-90,706,799 , GRCh38 (hg38) chr4: 89,785,648-89,785,648 SNCA
    nsv2306792short tandem repeat3nstd128human GRCh37 (hg19) chr4: 90,749,470-90,749,483 , GRCh38 (hg38) chr4: 89,828,319-89,828,332 SNCA
    nsv2306791short tandem repeat2nstd128human GRCh37 (hg19) chr4: 90,744,152-90,744,172 , GRCh38 (hg38) chr4: 89,823,001-89,823,021 SNCA
    nsv2306790short tandem repeat2nstd128human GRCh37 (hg19) chr4: 90,737,540-90,737,558 , GRCh38 (hg38) chr4: 89,816,389-89,816,407 SNCA
    nsv2306789short tandem repeat10nstd128human GRCh37 (hg19) chr4: 90,730,635-90,730,682 , GRCh38 (hg38) chr4: 89,809,484-89,809,531 SNCA
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