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Items: 1 to 20 of 242

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7076304inversion1nstd229human GRCh38 chr21: 31,661,410-31,663,931 , GRCh37.p13 chr21: 33,033,723-33,036,244 SOD1
    nsv7070554inversion1nstd229human GRCh38 chr21: 28,138,154-35,660,050 , GRCh37.p13 chr21: 29,510,473-37,032,348 , OR7E23P, 160 more genes
    nsv7070253inversion1nstd229human GRCh38 chr21: 28,377,443-35,730,342 , GRCh37.p13 chr21: 29,749,764-37,102,640 , HUNK, 161 more genes
    nsv7066273inversion1nstd229human GRCh38 chr21: 31,423,658-33,221,331 , GRCh37.p13 chr21: 32,795,971-34,593,636 MRAP, FBXW11P1, 37 more genes
    nsv7066036inversion1nstd229human GRCh38 chr21: 29,840,839-33,329,795 , GRCh37.p13 chr21: 31,213,156-34,702,101 SYNJ1, CLDN8, 95 more genes
    nsv7028180copy number variation1nstd229human GRCh38 chr21: 31,658,036-31,658,085 , GRCh37.p13 chr21: 33,030,349-33,030,398 SOD1-DT, SOD1
    nsv7024681copy number variation1nstd229human GRCh38 chr21: 31,038,501-31,675,400 , GRCh37.p13 chr21: 32,410,820-33,047,713 SOD1-DT, SCAF4, 9 more genes
    nsv7023286copy number variation1nstd229human GRCh38 chr21: 31,663,601-31,674,700 , GRCh37.p13 chr21: 33,035,914-33,047,013 SCAF4, SOD1
    nsv6634422copy number variation1nstd102humanUncertain significance GRCh37 chr21: 33,032,083-34,809,269 , GRCh38.p12 chr21: 31,659,770-33,436,962 SOD1, CFAP298, 39 more genes
    nsv6626624copy number variation1nstd224human GRCh37 chr21: 1-48,129,895 , GRCh38.p12 chr21: 8,522,361-46,699,983 , ATP5PO, 657 more genes
    nsv6596327inversion1nstd223human GRCh38 chr21: 28,377,391-35,730,332 , GRCh37.p13 chr21: 29,749,712-37,102,630 , LOC107985515, 161 more genes
    nsv6546109copy number variation1nstd223human GRCh38 chr21: 31,664,226-31,664,869 , GRCh37.p13 chr21: 33,036,539-33,037,182 SOD1
    nsv6315551copy number variation1nstd102humanPathogenic GRCh37 chr21: 14,420,615-48,080,926 , GRCh38.p12 chr21: 13,048,294-46,661,014 LTN1, LOC105372740, 622 more genes
    nsv6314196copy number variation1nstd102humanUncertain significance GRCh37 chr21: 27,185,913-35,853,445 , GRCh38.p12 chr21: 25,813,602-34,481,147 RPL12P9, CLDN17, 173 more genes
    nsv6313951copy number variation1nstd102humanPathogenic GRCh37 chr21: 15,041,209-48,097,372 , GRCh38.p12 chr21: 13,668,888-46,677,460 LOC107985515, ATP5PF, 606 more genes
    nsv6311248copy number variation2nstd102humanUncertain significance GRCh37 chr21: 32,439,271-39,212,984 , GRCh38.p12 chr21: 31,066,952-37,840,682 ATP5PO, LOC105372789, 131 more genes
    nsv6291538copy number variation1nstd102humanUncertain significance GRCh37 chr21: 32,676,376-35,131,913 , GRCh38.p12 chr21: 31,304,061-33,759,608 LINC00945, CFAP298-TCP10L, 53 more genes
    nsv6289996copy number variation1nstd102humanPathogenic GRCh37 chr21: 1-48,129,895 , GRCh38.p12 chr21: 8,522,361-46,699,983 KRTAP7-1, MAP3K7CL, 656 more genes
    nsv6278461copy number variation1nstd214human GRCh38 chr21: 31,658,035-31,658,084 , GRCh37.p13 chr21: 33,030,348-33,030,397 SOD1-DT, SOD1
    nsv6134323copy number variation1nstd213human GRCh37 chr21: 32,630,000-33,060,001 , GRCh38.p12 chr21: 31,257,684-31,687,688 SOD1, TIAM1, 7 more genes
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