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Items: 1 to 20 of 216

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7137085copy number variation1nstd102humanPathogenic GRCh37 chr5: 127,800,418-134,002,686 , GRCh38.p12 chr5: 128,464,725-134,666,996 CSF2, LOC402229, 99 more genes
    nsv7050047inversion1nstd229human GRCh38 chr5: 126,094,727-134,977,523 , GRCh37.p13 chr5: 125,430,420-134,313,213 RNU6-757P, SKP1, 145 more genes
    nsv7044234inversion1nstd229human GRCh38 chr5: 125,118,269-132,850,844 , GRCh37.p13 chr5: 124,453,962-132,186,536 RPLP1P7, IL4, 98 more genes
    nsv7042985inversion1nstd229human GRCh38 chr5: 129,885,016-134,639,437 , GRCh37.p13 chr5: 129,220,709-133,975,127 HSPA8P4, LINC02999, 85 more genes
    nsv7042749inversion1nstd229human GRCh38 chr5: 125,171,898-132,850,836 , GRCh37.p13 chr5: 124,507,591-132,186,528 LOC102723654, LOC105379174, 98 more genes
    nsv6797811copy number variation1nstd229human GRCh38 chr5: 131,172,636-131,184,177 , GRCh37.p13 chr5: 130,508,329-130,519,870 LYRM7
    nsv6796335copy number variation1nstd229human GRCh38 chr5: 130,976,570-131,254,856 , GRCh37.p13 chr5: 130,312,263-130,590,549 LOC105379172, RPL11P2, 3 more genes
    nsv6796294copy number variation1nstd229human GRCh38 chr5: 131,068,281-131,213,506 , GRCh37.p13 chr5: 130,403,974-130,549,199 LOC105379172, LYRM7, 1 more genes
    nsv6789527copy number variation1nstd229human GRCh38 chr5: 130,803,113-131,182,785 , GRCh37.p13 chr5: 130,138,806-130,518,478 HINT1, RPL11P2, 4 more genes
    nsv6789052copy number variation1nstd229human GRCh38 chr5: 131,181,640-131,216,131 , GRCh37.p13 chr5: 130,517,333-130,551,824 LYRM7
    nsv6787969copy number variation1nstd229human GRCh38 chr5: 131,068,191-131,213,509 , GRCh37.p13 chr5: 130,403,884-130,549,202 LOC105379172, HINT1, 1 more genes
    nsv6787766copy number variation1nstd229human GRCh38 chr5: 131,187,784-131,190,790 , GRCh37.p13 chr5: 130,523,477-130,526,483 LYRM7
    nsv6787056copy number variation1nstd229human GRCh38 chr5: 126,804,198-136,494,917 , GRCh37.p13 chr5: 126,139,890-135,830,606 SLC22A4, LOC105379199, 158 more genes
    nsv6786844copy number variation1nstd229human GRCh38 chr5: 131,172,392-131,263,108 , GRCh37.p13 chr5: 130,508,085-130,598,801 LYRM7, CDC42SE2
    nsv6782649copy number variation1nstd229human GRCh38 chr5: 131,193,118-131,199,684 , GRCh37.p13 chr5: 130,528,811-130,535,377 LYRM7
    nsv6636958copy number variation1nstd102humanUncertain significance GRCh37 chr5: 130,139,269-130,513,653 , GRCh38.p12 chr5: 130,803,576-131,177,960 LYRM7, LOC107986449, 4 more genes
    nsv6630052copy number variation1nstd224human GRCh37 chr5: 130,272,586-130,604,109 , GRCh38.p12 chr5: 130,936,893-131,268,416 HINT1, CDC42SE2, 4 more genes
    nsv6568194inversion1nstd223human GRCh38 chr5: 125,171,897-132,850,837 , GRCh37.p13 chr5: 124,507,590-132,186,529 LOC105379199, LMNB1, 98 more genes
    nsv6556353inversion1nstd223human GRCh38 chr5: 131,190,114-131,190,323 , GRCh37.p13 chr5: 130,525,807-130,526,016 LYRM7
    nsv6555891inversion1nstd223human GRCh38 chr5: 131,189,964-131,190,552 , GRCh37.p13 chr5: 130,525,657-130,526,245 LYRM7
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