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Items: 1 to 20 of 218

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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
    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
    nsv7045112inversion1nstd229human GRCh38 chr6: 30,561,326-37,907,708 , GRCh37.p13 chr6: 30,529,103-37,875,484 ZBTB22, PNPLA1, 355 more genes
    nsv6787643copy number variation1nstd229human GRCh38 chr6: 31,716,642-31,762,100 , GRCh37.p13 chr6: 31,684,419-31,729,877 DDAH2, LY6G6F-LY6G6D, 9 more genes
    nsv6781265copy number variation1nstd229human GRCh38 chr6: 31,746,927-31,747,017 , GRCh37.p13 chr6: 31,714,704-31,714,794 MSH5, MSH5-SAPCD1
    nsv6558790inversion1nstd223human GRCh38 chr6: 31,745,050-31,745,833 , GRCh37.p13 chr6: 31,712,827-31,713,610 MSH5-SAPCD1, MSH5
    nsv6403413copy number variation1nstd223human GRCh38 chr6: 31,731,185-31,756,579 , GRCh37.p13 chr6: 31,698,962-31,724,356 LOC105375020, RNU6-850P, 3 more genes
    nsv6402266copy number variation1nstd223human GRCh38 chr6: 31,522,086-32,653,908 , GRCh37.p13 chr6: 31,489,863-32,621,685 MIR6833, LY6G5B, 102 more genes
    nsv6304096copy number variation1nstd186human GRCh37 chr6: 31,717,808-31,717,985 , GRCh38.p12 chr6: 31,750,031-31,750,208 MSH5, MSH5-SAPCD1
    nsv6140608copy number variation1nstd206human GRCh38 chr6: 31,752,000-31,862,000 , GRCh37.p13 chr6: 31,719,777-31,829,777 LSM2, SLC44A4, 14 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
    nsv6010451copy number variation1nstd212human GRCh38 chr6: 31,745,016-31,745,071 , GRCh37.p13 chr6: 31,712,793-31,712,848 MSH5, MSH5-SAPCD1
    nsv5473312copy number variation1nstd206human GRCh38 chr6: 31,750,031-31,750,208 , GRCh37.p13 chr6: 31,717,808-31,717,985 MSH5-SAPCD1, MSH5
    nsv5467992copy number variation1nstd206human GRCh38 chr6: 31,745,882-31,746,934 , GRCh37.p13 chr6: 31,713,659-31,714,711 MSH5, MSH5-SAPCD1
    nsv5454592copy number variation1nstd206human GRCh38 chr6: 31,746,314-31,748,592 , GRCh37.p13 chr6: 31,714,091-31,716,369 MSH5, MSH5-SAPCD1
    nsv5234405copy number variation1nstd204human GRCh38.p13 chr6: 30,240,001-32,313,700 , GRCh37.p13 chr6: 30,207,778-32,281,477 DDAH2, LOC105375018, 175 more genes
    nsv5229879copy number variation1nstd204human GRCh38.p13 chr6: 31,502,001-32,151,900 , GRCh37.p13 chr6: 31,469,778-32,119,677 LTB, PPT2, 80 more genes
    nsv5229526copy number variation1nstd204human GRCh38.p13 chr6: 31,620,501-31,855,300 , GRCh37.p13 chr6: 31,588,278-31,823,077 LOC105375018, DDAH2, 35 more genes
    nsv4940692copy number variation1nstd200human GRCh38 chr6: 31,745,890-31,746,942 , GRCh37.p13 chr6: 31,713,667-31,714,719 MSH5-SAPCD1, MSH5
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