|
gptkb:16p11.2
|
chr16:29,550,000-30,100,000 (hg19)
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|
gptkb:chromosome_2q32
|
chr2:183,000,000-191,000,000 (approximate, GRCh38)
|
|
gptkb:chromosome_9p21
|
chr9:21,900,000-22,200,000 (GRCh38)
|
|
gptkb:chromosome_11q13.2
|
chr11:68,000,001-70,000,000 (GRCh38)
|
|
gptkb:Prader-Willi_syndrome_region
|
chr15:22,800,000-23,200,000 (hg19)
|
|
gptkb:chromosome_12p12.1_(KRAS)
|
chr12:25205246-25250937 (GRCh38)
|
|
gptkb:chromosome_7q31
|
chr7:113,000,000-117,000,000 (approximate)
|
|
gptkb:chromosome_7q22
|
chr7:100000000-110000000 (approximate)
|
|
gptkb:11p15.5
|
chr11:1-7,000,000 (approximate, GRCh38)
|
|
gptkb:chromosome_11q13
|
chr11:68,000,000-70,000,000 (approximate)
|
|
gptkb:22q11.21
|
chr22:18,800,000-21,500,000 (GRCh38)
|
|
gptkb:Xp22.3
|
NCBI GRCh38: 2,700,001-8,800,000
|
|
gptkb:20q13.2
|
chr20:50,000,000-56,000,000 (approximate)
|
|
gptkb:11p15.3
|
chr11:1-25,000,000 (approximate)
|
|
gptkb:chromosome_18q12.3_(human)
|
chr18: 38,000,001-41,000,000 (GRCh38)
|
|
gptkb:chromosome_22q11.21
|
chr22:18,800,000-21,500,000 (GRCh38)
|
|
gptkb:16p12.1
|
chr16:21,900,000-22,600,000 (GRCh38)
|
|
gptkb:chromosome_5q35.3
|
chr5:176,000,001-180,915,260 (GRCh38)
|
|
gptkb:chromosome_4q27
|
chr4:123,000,000-123,500,000 (approximate, hg19)
|
|
gptkb:chromosome_11q22.3
|
chr11:108,100,000-111,600,000 (GRCh38)
|