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Items: 1 to 20 of 126

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7096974copy number variation1nstd102humanUncertain significance GRCh37 chr4: 121,616,266-124,323,706 , GRCh38.p12 chr4: 120,695,111-123,402,551 RN7SL335P, QRFPR, 40 more genes
    nsv7052550inversion1nstd229human GRCh38 chr4: 122,697,186-122,740,643 , GRCh37.p13 chr4: 123,618,341-123,661,798 BBS12, LOC727709, 1 more genes
    nsv7051830inversion1nstd229human GRCh38 chr4: 122,021,125-125,223,020 , GRCh37.p13 chr4: 122,942,280-126,144,175 SPRY1, ANKRD50, 29 more genes
    nsv7046719inversion1nstd229human GRCh38 chr4: 122,720,397-122,746,444 , GRCh37.p13 chr4: 123,641,552-123,667,599 BBS12, LOC727709, 1 more genes
    nsv7046043inversion1nstd229human GRCh38 chr4: 121,571,489-125,148,298 , GRCh37.p13 chr4: 122,492,644-126,069,453 TRC-GCA2-1, LINC02435, 39 more genes
    nsv7043432inversion1nstd229human GRCh38 chr4: 117,041,189-125,064,058 , GRCh37.p13 chr4: 117,962,345-125,985,213 SEPTIN14P4, LINC02516, 109 more genes
    nsv7040293inversion1nstd229human GRCh38 chr4: 122,406,938-123,167,062 , GRCh37.p13 chr4: 123,328,093-124,088,217 IL21-AS1, NUDT6, 11 more genes
    nsv6754528copy number variation1nstd229human GRCh38 chr4: 122,606,959-123,206,244 , GRCh37.p13 chr4: 123,528,114-124,127,399 BBS12, RPS26P23, 9 more genes
    nsv6570561inversion1nstd223human GRCh38 chr4: 117,041,188-125,064,052 , GRCh37.p13 chr4: 117,962,344-125,985,207 MYOZ2, NT5C3AP1, 109 more genes
    nsv6313878copy number variation1nstd102humanPathogenic GRCh37 chr4: 104,715,235-145,252,595 , GRCh38.p12 chr4: 103,794,078-144,331,443 LINC00613, GYPA, 448 more genes
    nsv6313750copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,888,785-129,649,979 , GRCh38.p12 chr4: 115,967,629-128,728,824 LOC105377395, SEPTIN7P14, 152 more genes
    nsv6291432copy number variation1nstd102humanPathogenic GRCh37 chr4: 52,866,944-143,582,507 , GRCh38.p12 chr4: 52,000,778-142,661,354 SNHG27, TNIP3, 1091 more genes
    nsv6290265copy number variation1nstd102humanPathogenic GRCh37 chr4: 114,872,547-138,005,267 , GRCh38.p12 chr4: 113,951,391-137,084,113 LOC105379404, IL21-AS1, 218 more genes
    nsv6134886copy number variation1nstd213human GRCh37 chr4: 121,830,000-124,220,001 , GRCh38.p12 chr4: 120,908,845-123,298,846 ANXA5, CCNA2, 36 more genes
    nsv6134884copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,720,001 , GRCh38.p12 chr4: 108,308,844-160,798,849 , ANK2, 616 more genes
    nsv6134731copy number variation1nstd213human GRCh37 chr4: 109,230,000-161,710,001 , GRCh38.p12 chr4: 108,308,844-160,788,849 , ANK2, 616 more genes
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5558253sequence alteration1nstd206human GRCh38 chr4: 120,373,769-143,797,136 , GRCh37.p13 chr4: 121,294,924-144,718,289 , IL15, 218 more genes
    nsv5381774copy number variation1nstd102humanPathogenic GRCh37 chr4: 116,833,638-130,232,122 , GRCh38.p12 chr4: 115,912,482-129,310,967 LOC112268469, LOC105377393, 159 more genes
    nsv4935651copy number variation1nstd200human GRCh38 chr4: 122,728,034-122,728,660 , GRCh37.p13 chr4: 123,649,189-123,649,815 BBS12, CETN4P
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