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Items: 1 to 20 of 180

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7098938copy number variation1nstd102humanUncertain significance GRCh38 chr7: 116,868,268-117,565,389 , GRCh37.p13 chr7: 116,508,322-117,205,443 ST7-AS1, MTND2P37, 20 more genes
    nsv7047324inversion1nstd229human GRCh38 chr7: 117,292,185-117,294,638 , GRCh37.p13 chr7: 116,932,239-116,934,692 LOC105375467, WNT2
    nsv6832425copy number variation1nstd229human GRCh38 chr7: 117,272,101-117,276,400 , GRCh37.p13 chr7: 116,912,155-116,916,454 WNT2
    nsv6831475copy number variation1nstd229human GRCh38 chr7: 110,527,230-117,297,230 , GRCh37.p13 chr7: 110,167,287-116,937,284 IMMP2L, LOC105375466, 66 more genes
    nsv6829415copy number variation1nstd229human GRCh38 chr7: 117,320,216-117,367,535 , GRCh37.p13 chr7: 116,960,270-117,007,589 LOC105375467, ASZ1, 1 more genes
    nsv6828401copy number variation1nstd229human GRCh38 chr7: 117,244,211-117,732,134 , GRCh37.p13 chr7: 116,884,265-117,372,188 ASZ1, LOC105375467, 10 more genes
    nsv6827180copy number variation1nstd229human GRCh38 chr7: 116,747,495-117,319,278 , GRCh37.p13 chr7: 116,387,549-116,959,332 LOC105375467, CAPZA2, 16 more genes
    nsv6819444copy number variation1nstd229human GRCh38 chr7: 117,303,739-117,331,368 , GRCh37.p13 chr7: 116,943,793-116,971,422 LOC105375467, WNT2
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6615866copy number variation1nstd223human GRCh38 chr7: 117,292,362-117,294,169 , GRCh37.p13 chr7: 116,932,416-116,934,223 WNT2, LOC105375467
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6314995copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 114,885,745-124,728,629 , GRCh38.p12 chr7: 115,245,691-125,088,575 CAPZA2, CAV1, 109 more genes
    nsv6313851copy number variation1nstd102humanPathogenic GRCh37 chr7: 106,984,287-128,949,489 , GRCh38.p12 chr7: 107,343,842-129,309,648 DOCK4-AS1, RPL3P8, 262 more genes
    nsv6313576copy number variation1nstd102humanPathogenic GRCh37 chr7: 100,676,872-119,156,160 , GRCh38.p12 chr7: 101,033,591-119,516,106 LHFPL3-AS2, CTB-30L5.1, 233 more genes
    nsv6239623mobile element insertion1nstd215human GRCh38 chr7: 117,316,692-117,316,692 , GRCh37.p13 chr7: 116,956,746-116,956,746 WNT2, LOC105375467
    nsv6136542copy number variation1nstd213human GRCh37 chr7: 116,240,000-116,990,001 , GRCh38.p12 chr7: 116,599,946-117,349,947 ST7-AS1, ST7-OT4, 17 more genes
    nsv6136533copy number variation1nstd213human GRCh37 chr7: 104,130,000-120,060,001 , GRCh38.p12 chr7: 104,489,552-120,419,947 CAPZA2, CFTR, 162 more genes
    nsv6135954copy number variation1nstd213human GRCh37 chr7: 114,370,000-117,780,001 , GRCh38.p12 chr7: 114,729,945-118,139,947 TFEC, TES, 40 more genes
    nsv6135872copy number variation1nstd213human GRCh37 chr7: 113,230,000-128,010,001 , GRCh38.p12 chr7: 113,589,945-128,369,947 CAV1, SLC13A1, 154 more genes
    nsv5558718sequence alteration1nstd206human GRCh38 chr7: 117,292,184-117,294,631 , GRCh37.p13 chr7: 116,932,238-116,934,685 WNT2, LOC105375467
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