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Items: 1 to 20 of 149

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7043432inversion1nstd229human GRCh38 chr4: 117,041,189-125,064,058 , GRCh37.p13 chr4: 117,962,345-125,985,213 SEPTIN14P4, LINC02516, 109 more genes
    nsv6756423copy number variation1nstd229human GRCh38 chr4: 119,303,379-119,400,972 , GRCh37.p13 chr4: 120,224,534-120,322,127 LOC107986193, GK6P, 4 more genes
    nsv6750652copy number variation1nstd229human GRCh38 chr4: 119,298,780-119,300,335 , GRCh37.p13 chr4: 120,219,935-120,221,490 C4orf3
    nsv6745071copy number variation1nstd229human GRCh38 chr4: 119,287,387-119,359,206 , GRCh37.p13 chr4: 120,208,542-120,280,361 USP53, FABP2, 2 more genes
    nsv6742442copy number variation1nstd229human GRCh38 chr4: 119,296,264-119,296,360 , GRCh37.p13 chr4: 120,217,419-120,217,515 C4orf3
    nsv6739019copy number variation1nstd229human GRCh38 chr4: 119,296,609-119,299,470 , GRCh37.p13 chr4: 120,217,764-120,220,625 C4orf3
    nsv6629094copy number variation1nstd224human GRCh37 chr4: 120,214,030-120,277,395 , GRCh38.p12 chr4: 119,292,875-119,356,240 USP53, KLHL2P1, 2 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
    nsv6383699copy number variation1nstd223human GRCh38 chr4: 119,233,849-119,330,597 , GRCh37.p13 chr4: 120,155,004-120,251,752 FABP2, USP53, 1 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
    nsv6313717copy number variation1nstd102humanUncertain significance GRCh37 chr4: 119,902,254-121,463,237 , GRCh38.p12 chr4: 118,981,099-120,542,082 LOC102723967, PDE5A, 26 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
    nsv6135278copy number variation1nstd213human GRCh37 chr4: 120,100,000-120,280,001 , GRCh38.p12 chr4: 119,178,845-119,358,846 FABP2, MYOZ2, 5 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
    nsv6074774insertion1nstd212human GRCh38 chr4: 119,296,228-119,296,228 , GRCh37.p13 chr4: 120,217,383-120,217,383 C4orf3
    nsv5562145sequence alteration1nstd206human GRCh38 chr4: 74,717,205-184,730,527 , GRCh37.p13 chr4: 75,689,880-185,651,681 , ASS1P8, 1307 more genes
    nsv5468408copy number variation1nstd206human GRCh38 chr4: 119,303,930-119,328,528 , GRCh37.p13 chr4: 120,225,085-120,249,683 C4orf3, FABP2
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