GRCh38/hg38 5q11.2-13.2(chr5:58785203-73519962)x1 Detail (hg38) (TRIM23, BTF3, CCNB1, CDK7, ERCC8, FOXD1, GTF2H2, HTR1A, KIF2A, TNPO1, CD180, MAP1B, NAIP, PDE4D, PIK3R1, RAD17, SMN1, SMN2, TAF9, SERF1A, CARTPT, CWC27, ADAMTS6, MRPS27, PPWD1, PART1, DIMT1, IPO11, SGTB, DEPDC1B, BDP1, ERBIN, NLN, ZSWIM6, MCCC2, CENPK, SLC30A5, CENPH, PTCD2, ELOVL7, TRAPPC13, NDUFAF2, KGD4, FCHO2, RAB3C, TMEM171, TMEM174, SREK1, MARVELD2, ZNF366, CCDC125, LINC03122, RNF180, SREK1IP1, LOC340090, MAST4, RGS7BP, SMIM15, MIR582, GTF2H2C, SERF1B, LRRC70, SHISAL2B, LINC03123, OCLN, MIR4804, MIR4803, IPO11-LRRC70, SMIM15-AS1, LOC101928651, LINC02065, LINC02229, MAST4-AS1, LINC02997, LINC02198, LOC101928924, AK6, LINC02219, LOC102503427, LINC02197, LINC01386, ERCC8-AS1, LINC02057, LOC105378997, LINC02242, LOC105379030, LINC02230, SNORA50D, SNORD13B-1, SNORD13B-2, LOC111089946, LOC111556106, SHLD3, LOC113002588, LOC113002589, LOC113002590, LOC113002591, LOC114004394, LOC116158518, BTF3-DT, FCHO2-DT, LOC121079939, LOC121079940, LOC121079941, LOC121079942, LOC121079943, LOC121079944, LOC121079945, TNPO1-DT, LOC121725205, LOC121725206, LOC121725207, LOC123493319, LOC123493320, LOC123493321, LOC123493322, LOC123493323, LOC123493324, LOC123493325, LOC123493326, LOC123493327, LOC123493329, LOC123493330, LOC123493331, LOC123493332, LOC123493333, LOC123493334, LOC123493335, LOC123497905, LOC123497906, TILRLS, LOC126807403, LOC126807404, LOC126807405, LOC126807406, LOC126807407, LOC126807408, LOC126807409, LOC126807410, LOC126807411, LOC126807412, LOC126807413, LOC126807414, LOC126807415, LOC126807416, LOC126807417, LOC126807418, LOC126807419, LOC129389287, LOC129389288, LOC129389289, LOC129389290, LOC129389291, LOC129389292, LOC129389293, LOC129389294, LOC129389296, LOC129993938, LOC129993939, LOC129993940, LOC129993941, LOC129993942, LOC129993943, LOC129993944, LOC129993945, LOC129993946, LOC129993947, LOC129993948, LOC129993949, LOC129993950, LOC129993951, LOC129993952, LOC129993953, LOC129993954, LOC129993955, LOC129993956, LOC129993957, LOC129993958, LOC129993959, LOC129993960, LOC129993961, LOC129993962, LOC129993963, LOC129993964, LOC129993965, LOC129993966, LOC129993967, LOC129993968, LOC129993969, LOC129993970, LOC129993971, LOC129993972, LOC129993973, LOC129993974, LOC129993975, LOC129993976, LOC129993977, LOC129993978, LOC129993979, LOC129993980, LOC129993981, LOC129993982, LOC129993983, LOC129993984, LOC129993985, LOC129993986, LOC129993987, LOC129993988, LOC129993989, LOC129993990, LOC129993991, LOC129993992, LOC129993993, LOC129993994, LOC129993995, LOC129993996, LOC129993997, LOC129993998, LOC129993999, LOC129994000, LOC129994001, LOC129994002, LOC129994003, LOC129994004, LOC129994005, LOC129994006, LOC129994007, LOC129994008, LOC129994009, LOC129994010, LOC129994011, LOC129994012, LOC129994013, LOC129994014, LOC129994015, LOC129994016, LOC129994017, LOC129994018, LOC129994019, LOC129994020, LOC129994021, LOC129994022, LOC129994023, LOC129994024, LOC129994025, LOC129994026, LOC129994027, LOC129994028, LOC129994029, LOC129994030, LOC129994031, LOC129994032, LOC129994033, LOC129994034, LOC129994035, LOC129994036, LOC129994037, LOC129994038, LOC129994039, LOC129994040, LOC129994041, LOC129994042, LOC129994043, LOC129994044, LOC129994045, SMN-AS1, LOC132089288)
Information
Genome
Assembly | Position |
---|---|
hg19 | chr5:58,076,468-72,819,205 |
hg38 | chr5:58,780,641-73,523,380 |
Summary
MGeND
Clinical significance | |
Variant entry | |
GWAS entry | |
Disease area statistics | Show details |
ClinVar
Clinical Significance |
![]() |
Review star | ![]() |
Show details |
Links
Type | Database | ID | Link |
---|---|---|---|
Gene | MIM | ||
HGNC | |||
Ensembl | |||
NCBI | |||
Gene Cards | |||
OncoKB |
Type | Database | ID | Link |
---|---|---|---|
Variant | TogoVar | ||
COSMIC | |||
MONDO |
Disease area statistics
[No Data.]
MGeND
[No Data.]
ClinVar
Clinical significance | Last evaluated | Review status | Condition | Origin | Links |
---|---|---|---|---|---|
![]() |
no assertion criteria provided | intellectual disability |
![]() |
Detail |
CIViC
[No Data.]
DisGeNET
[No Data.]
Annotation
Annotations
Descrption | Source | Links |
---|---|---|
GRCh38/hg38 5q11.2-13.2(chr5:58785203-73519962)x1 AND Intellectual disability | ClinVar | Detail |
Overlapped Transcript Coordinates
Gene | Transcript ID | Exon Number | Chromosome | Start | Stop | Type | Amino Mutation | Transcript Position | Links |
---|
Overlapped Transcript
Gene | Transcript ID | Chromosome | Start | Stop | Links |
---|
- Gene
- -
- Genome
- hg38
- Position
- chr5:58,780,641-73,523,380
- Variant Type
- cnv
Genome browser