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Items: 1 to 20 of 151

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7146159insertion1nstd232human GRCh37.p13 chr5: 137,427,517-137,427,517 , GRCh38.p12 chr5: 138,091,828-138,091,828 WNT8A
    nsv7097022copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-138,861,289 , GRCh38.p12 chr5: 137,622,098-139,481,704 CDC25C, SLC23A1, 55 more genes
    nsv7096751copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-140,078,137 , GRCh38.p12 chr5: 137,622,098-140,698,552 CDC25C, LOC100128966, 94 more genes
    nsv6795261copy number variation1nstd229human GRCh38 chr5: 138,092,299-138,099,411 , GRCh37.p13 chr5: 137,427,988-137,435,100 WNT8A
    nsv6793835copy number variation1nstd229human GRCh38 chr5: 138,039,501-138,538,500 , GRCh37.p13 chr5: 137,375,190-137,874,189 RNU6-460P, RNU6-1148P, 17 more genes
    nsv6785976copy number variation1nstd229human GRCh38 chr5: 138,035,187-138,098,373 , GRCh37.p13 chr5: 137,370,876-137,434,062 FAM13B, FAM13B-AS1, 2 more genes
    nsv6560833inversion1nstd223human GRCh38 chr5: 138,087,646-138,088,375 , GRCh37.p13 chr5: 137,423,335-137,424,064 WNT8A
    nsv6560661inversion1nstd223human GRCh38 chr5: 138,076,074-138,076,823 , GRCh37.p13 chr5: 137,411,763-137,412,512 WNT8A
    nsv6409477copy number variation1nstd223human GRCh38 chr5: 138,081,046-138,082,829 , GRCh37.p13 chr5: 137,416,735-137,418,518 WNT8A
    nsv6405600copy number variation1nstd223human GRCh38 chr5: 137,606,101-142,582,700 , GRCh37.p13 chr5: 136,941,790-141,962,265 TMCO6, PCDHB17P, 191 more genes
    nsv6400333copy number variation1nstd223human GRCh38 chr5: 138,071,509-138,086,942 , GRCh37.p13 chr5: 137,407,198-137,422,631 WNT8A
    nsv6313595copy number variation1nstd102humanPathogenic GRCh37 chr5: 132,031,902-137,623,639 , GRCh38.p12 chr5: 132,696,210-138,287,950 TGFBI, RPS10P11, 110 more genes
    nsv6278192insertion1nstd214human GRCh38 chr5: 138,091,828-138,091,828 , GRCh37.p13 chr5: 137,427,517-137,427,517 WNT8A
    nsv6182376copy number variation1nstd214human GRCh38 chr5: 138,079,299-138,079,358 , GRCh37.p13 chr5: 137,414,988-137,415,047 WNT8A
    nsv6135383copy number variation1nstd213human GRCh37 chr5: 137,050,000-138,100,001 , GRCh38.p12 chr5: 137,714,311-138,764,312 CDC25C, CTNNA1, 32 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6135115copy number variation1nstd213human GRCh37 chr5: 137,330,000-138,340,001 , GRCh38.p12 chr5: 137,994,311-139,004,312 HSPA9, KIF20A, 27 more genes
    nsv6079264insertion1nstd212human GRCh38 chr5: 138,079,554-138,079,554 , GRCh37.p13 chr5: 137,415,243-137,415,243 WNT8A
    nsv6067368insertion1nstd212human GRCh38 chr5: 138,091,828-138,091,828 , GRCh37.p13 chr5: 137,427,517-137,427,517 WNT8A
    nsv6006231copy number variation1nstd212human GRCh38 chr5: 138,075,930-138,075,985 , GRCh37.p13 chr5: 137,411,619-137,411,674 WNT8A
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