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Items: 1 to 20 of 181

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097426copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-36,953,949 , GRCh38.p12 chr6: 30,728,116-36,986,173 LEMD2, PSORS1C1, 321 more genes
    nsv7097327copy number variation1nstd102humanPathogenic GRCh37 chr6: 30,890,861-30,892,357 , GRCh38.p12 chr6: 30,923,084-30,924,580 VARS2
    nsv7097325copy number variation1nstd102humanUncertain significance GRCh37 chr6: 30,695,893-31,937,492 , GRCh38.p12 chr6: 30,728,116-31,969,715 HCG21, SNORD84, 117 more genes
    nsv7053830inversion1nstd229human GRCh38 chr6: 29,164,448-38,692,657 , GRCh37.p13 chr6: 29,132,225-38,660,433 GTF2H4, RNF8, 472 more genes
    nsv7050588inversion1nstd229human GRCh38 chr6: 30,920,282-30,924,832 , GRCh37.p13 chr6: 30,888,059-30,892,609 VARS2
    nsv7045629inversion1nstd229human GRCh38 chr6: 30,007,594-31,355,527 , GRCh37.p13 chr6: 29,975,371-31,323,304 USP8P1, LINC02571, 82 more genes
    nsv7045112inversion1nstd229human GRCh38 chr6: 30,561,326-37,907,708 , GRCh37.p13 chr6: 30,529,103-37,875,484 ZBTB22, PNPLA1, 355 more genes
    nsv6797863copy number variation1nstd229human GRCh38 chr6: 30,918,656-30,918,797 , GRCh37.p13 chr6: 30,886,433-30,886,574 VARS2
    nsv6795673copy number variation1nstd229human GRCh38 chr6: 30,444,101-31,201,100 , GRCh37.p13 chr6: 30,411,878-31,168,877 POU5F1, DDR1, 51 more genes
    nsv6794247copy number variation1nstd229human GRCh38 chr6: 30,380,601-31,245,000 , GRCh37.p13 chr6: 30,348,378-31,212,777 MUC22, TMPOP1, 52 more genes
    nsv6790873copy number variation1nstd229human GRCh38 chr6: 30,888,982-31,005,512 , GRCh37.p13 chr6: 30,856,759-30,973,289 HCG21, MUCL3, 8 more genes
    nsv6562568inversion1nstd223human GRCh38 chr6: 29,766,029-31,471,345 , GRCh37.p13 chr6: 29,733,806-31,439,122 HCG4P9, LINC01149, 126 more genes
    nsv6314918copy number variation1nstd102humanUncertain significance GRCh38 chr6: 30,888,982-31,005,512 , GRCh37.p13 chr6: 30,856,759-30,973,289 MUC21, MIR4640, 8 more genes
    nsv6289880copy number variation1nstd102humanLikely pathogenic GRCh37 chr6: 28,005,012-31,683,185 , GRCh38.p12 chr6: 28,037,234-31,715,408 ABCF1, AIF1, 313 more genes
    nsv6185006copy number variation1nstd214human GRCh38 chr6: 30,918,653-30,918,792 , GRCh37.p13 chr6: 30,886,430-30,886,569 VARS2
    nsv6135918copy number variation1nstd213human GRCh37 chr6: 30,870,000-31,240,001 , GRCh38.p12 chr6: 30,902,223-31,272,224 CDSN, GTF2H4, 19 more genes
    nsv6135917copy number variation1nstd213human GRCh37 chr6: 30,110,000-32,450,001 , GRCh38.p12 chr6: 30,142,223-32,482,224 ABCF1, AGER, 186 more genes
    nsv6002190copy number variation1nstd212human GRCh38 chr6: 30,918,653-30,918,793 , GRCh37.p13 chr6: 30,886,430-30,886,570 VARS2
    nsv5582980copy number variation1nstd207human GRCh38 chr6: 30,918,653-30,918,792 , GRCh37.p13 chr6: 30,886,430-30,886,569 VARS2
    nsv5465972copy number variation1nstd206human GRCh38 chr6: 30,888,982-31,005,512 , GRCh37.p13 chr6: 30,856,759-30,973,289 MUC22, HCG21, 8 more genes
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