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Items: 1 to 20 of 123

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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
    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
    nsv6741174copy number variation1nstd229human GRCh38 chr4: 121,737,689-121,765,764 , GRCh37.p13 chr4: 122,658,844-122,686,919 PP12613, SMIM43
    nsv6741047copy number variation1nstd229human GRCh38 chr4: 121,655,546-121,871,460 , GRCh37.p13 chr4: 122,576,701-122,792,615 SMIM43, BBS7, 4 more genes
    nsv6739735copy number variation1nstd229human GRCh38 chr4: 121,745,676-122,710,918 , GRCh37.p13 chr4: 122,666,831-123,632,073 CCNA2, TRPC3, 13 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
    nsv6382547copy number variation1nstd223human GRCh38 chr4: 121,760,501-121,767,000 , GRCh37.p13 chr4: 122,681,656-122,688,155 SMIM43, PP12613
    nsv6382275copy number variation1nstd223human GRCh38 chr4: 121,625,271-122,343,784 , GRCh37.p13 chr4: 122,546,426-123,264,939 LOC112268469, CCNA2, 10 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
    nsv6135281copy number variation1nstd213human GRCh37 chr4: 122,550,000-122,800,001 , GRCh38.p12 chr4: 121,628,845-121,878,846 ANXA5, CCNA2, 6 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
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