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Items: 1 to 20 of 192

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv6112754copy number variation1nstd102humanPathogenic GRCh37 chr4: 131,303,317-168,722,402 , GRCh38.p12 chr4: 130,382,162-167,801,251 MIR3139, CLGN, 407 more genes
    nsv5613230insertion1nstd207human GRCh38 chr4: 139,289,132-139,289,132 , GRCh37.p13 chr4: 140,210,286-140,210,286 NDUFC1
    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
    nsv5324341inversion1nstd204human GRCh37.p13 chr4: 137,941,712-143,237,910 , GRCh38.p13 chr4: 137,020,558-142,316,757 , ELF2, 68 more genes
    nsv5313810copy number variation1nstd204human GRCh37.p13 chr4: 140,042,236-140,229,630 , GRCh38.p13 chr4: 139,121,082-139,308,476 ELF2, NDUFC1, 6 more genes
    nsv5239971copy number variation1nstd204human GRCh37.p13 chr4: 140,042,455-140,228,854 , GRCh38.p13 chr4: 139,121,301-139,307,700 ELF2, NDUFC1, 6 more genes
    nsv5231235copy number variation1nstd204human GRCh38.p13 chr4: 139,298,762-139,307,522 , GRCh37.p13 chr4: 140,219,916-140,228,676 NDUFC1, NAA15
    nsv5229565copy number variation1nstd204human GRCh38.p13 chr4: 139,294,443-139,295,442 , GRCh37.p13 chr4: 140,215,597-140,216,596 NDUFC1
    nsv5099563mobile element insertion1nstd203human GRCh38 chr4: 139,289,123-139,289,148 , GRCh37.p13 chr4: 140,210,277-140,210,302 NDUFC1
    nsv5096936mobile element insertion1nstd203human GRCh38 chr4: 139,289,132-139,289,148 , GRCh37.p13 chr4: 140,210,286-140,210,302 NDUFC1
    nsv5093529mobile element insertion1nstd203human GRCh38 chr4: 139,289,137-139,289,148 , GRCh37.p13 chr4: 140,210,291-140,210,302 NDUFC1
    nsv5092573mobile element insertion1nstd203human GRCh38 chr4: 139,289,136-139,289,148 , GRCh37.p13 chr4: 140,210,290-140,210,302 NDUFC1
    nsv5090738mobile element insertion1nstd203human GRCh38 chr4: 139,293,827-139,293,843 , GRCh37.p13 chr4: 140,214,981-140,214,997 NDUFC1
    nsv5090362mobile element insertion1nstd203human GRCh38 chr4: 139,289,088-139,289,148 , GRCh37.p13 chr4: 140,210,242-140,210,302 NDUFC1
    nsv5087547mobile element insertion1nstd203human GRCh38 chr4: 139,289,145-139,289,148 , GRCh37.p13 chr4: 140,210,299-140,210,302 NDUFC1
    nsv5087380mobile element insertion1nstd203human GRCh38 chr4: 139,289,144-139,289,147 , GRCh37.p13 chr4: 140,210,298-140,210,301 NDUFC1
    nsv5086441mobile element insertion1nstd203human GRCh38 chr4: 139,289,120-139,289,148 , GRCh37.p13 chr4: 140,210,274-140,210,302 NDUFC1
    nsv5086356mobile element insertion1nstd203human GRCh38 chr4: 139,289,148-139,289,181 , GRCh37.p13 chr4: 140,210,302-140,210,335 NDUFC1
    nsv5083098mobile element insertion1nstd203human GRCh38 chr4: 139,289,116-139,289,132 , GRCh37.p13 chr4: 140,210,270-140,210,286 NDUFC1
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