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Items: 1 to 20 of 262

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7139873copy number variation1nstd232human GRCh37.p13 chr7: 128,492,805-128,492,879 , GRCh38.p12 chr7: 128,852,751-128,852,825 FLNC, FLNC-AS1
    nsv7097862copy number variation1nstd102humanUncertain significance GRCh37 chr7: 128,470,692-128,482,448 , GRCh38.p12 chr7: 128,830,638-128,842,394 FLNC
    nsv7097483copy number variation1nstd102humanPathogenic GRCh37 chr7: 128,480,619-128,486,474 , GRCh38.p12 chr7: 128,840,565-128,846,420 FLNC
    nsv7097482copy number variation1nstd102humanLikely pathogenic GRCh37 chr7: 128,480,199-128,481,774 , GRCh38.p12 chr7: 128,840,145-128,841,720 FLNC
    nsv7097481copy number variation1nstd102humanPathogenic GRCh37 chr7: 128,475,360-128,478,877 , GRCh38.p12 chr7: 128,835,306-128,838,823 FLNC
    nsv7097480copy number variation1nstd102humanPathogenic GRCh37 chr7: 128,470,692-128,498,577 , GRCh38.p12 chr7: 128,830,638-128,858,523 FLNC, FLNC-AS1
    nsv7093224copy number variation1nstd102humanPathogenic GRCh37 chr7: 128,497,170-128,497,171 , GRCh38 chr7: 128,857,116-128,857,117 FLNC, FLNC-AS1
    nsv7054280inversion1nstd229human GRCh38 chr7: 128,104,928-130,077,832 , GRCh37.p13 chr7: 127,744,980-129,717,672 CICP14, RNA5SP243, 63 more genes
    nsv7047961inversion1nstd229human GRCh38 chr7: 123,155,784-130,261,366 , GRCh37.p13 chr7: 122,795,838-129,901,206 IQUB, LOC107986843, 122 more genes
    nsv7047247inversion1nstd229human GRCh38 chr7: 123,130,391-130,261,365 , GRCh37.p13 chr7: 122,770,445-129,901,205 RNA5SP244, RNA5SP243, 122 more genes
    nsv7046115inversion1nstd229human GRCh38 chr7: 128,204,685-135,838,306 , GRCh37.p13 chr7: 127,844,738-135,523,054 RPL37P16, BPGM, 155 more genes
    nsv7043190inversion1nstd229human GRCh38 chr7: 123,472,699-130,834,800 , GRCh37.p13 chr7: 123,112,753-129,984,423 KCP, LINC01000, 138 more genes
    nsv6837835copy number variation1nstd229human GRCh38 chr7: 128,205,538-135,806,503 , GRCh37.p13 chr7: 127,845,591-135,491,251 RN7SL81P, IMP3P2, 155 more genes
    nsv6837736copy number variation1nstd229human GRCh38 chr7: 128,633,501-128,974,300 , GRCh37.p13 chr7: 128,273,555-128,614,354 FLNC, KCP, 20 more genes
    nsv6829719copy number variation1nstd229human GRCh38 chr7: 128,840,751-128,840,786 , GRCh37.p13 chr7: 128,480,805-128,480,840 FLNC
    nsv6826847copy number variation1nstd229human GRCh38 chr7: 128,830,601-128,974,300 , GRCh37.p13 chr7: 128,470,655-128,614,354 TNPO3, IRF5, 8 more genes
    nsv6826437copy number variation1nstd229human GRCh38 chr7: 128,759,901-128,974,300 , GRCh37.p13 chr7: 128,399,955-128,614,354 TRP-AGG2-3, CALU, 13 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6313876copy number variation1nstd102humanPathogenic GRCh37 chr7: 124,103,982-134,693,590 , GRCh38.p12 chr7: 124,463,928-135,008,839 IMPDH1, SSU72L6, 174 more genes
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